2’635 Firmen für deine Suche.

Novartis AG

Novartis bietet innovative medizinische Lösungen an, um damit auf die sich verändernden Bedürfnisse von Patienten und Gesellschaften einzugehen. Novartis, mit Hauptsitz in Basel (Schweiz), verfügt über ein diversifiziertes Portfolio, um diese Bedürfnisse so gut wie möglich zu erfüllen: mit innovativen Arzneimitteln, Produkten für die Augenheilkunde und kostengünstigen generischen Medikamenten. Novartis ist das einzige Unternehmen mit weltweit führenden Positionen in diesen Bereichen.

Novartis AG

Fabrikstrasse 2
4056Basel

20.02.2020

Novartis AG

Post Doc

  • Novartis AG

  • 4040Basel

  • 20.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID290092BRPosition TitlePost DocApply to Job Job Description For the Viral Vectors Development Team, Cell and Gene Therapy Technical Development Unit within Technical Research and Development, we are looking for a Post Doc to explore innovative strategies for the development of formulations and drug product processes for viral vector based products. Plan, perform and lead dedicated R&D work for: - Development of formulations for gene therapy - Systematical evaluation of new concepts and screening of novel excipients for vector formulation (e.g. AAV and LVs) - Evaluation of critical process parameters and primary packaging suitable for viral vectors Actively participate in internal discussions, present results internally. - Write internal reports, lab documentation and protocols - Contribute to new IP opportunities and/or scientific publications. - Project outcomes will support the implementation of new strategies to enable early development of special formulations for the gene therapies biologics pipeline. Minimum requirements PhD in Pharmaceutical Sciences, Biotechnologies, Life Sciences or equivalent. Prior knowledge and experience with viral vectors is desirable. Familiar with formulation technologies for biologics. Fluent in English Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

20.02.2020

Novartis AG

Administrative Professional

  • Novartis AG

  • 4051Basel

  • 20.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID290106BRPosition TitleAdministrative ProfessionalApply to Job Job Description We are looking for an Administrative Professional who supports the Pharma Division Management Office. You will be responsible for managing complex administrative and organizational assignments in the global field. Your responsibilities: Your responsibilities include, but are not limited to: General organizational support: • Deal with complex administrative & organizational assignments independently and take care of general admin tasks, e.g. dealing with and replying to correspondence, filing, appointment / deadline coordination, database administration • Supervising demanding processes, e.g. target/actual comparisons, budget, checking and assigning invoices • Preparing presentations after prior discussion of content, preparation and evaluation of statistics, meeting preparation and taking minutes Interaction: • Inform, advise and support the team and associates from outside the team on processes, guidelines and services that are specific to the department Work processes in own area of responsibility: • Initiate/modify processes and coordinate their introduction Handling of administrative projects: • Acts as project coordinator/manager for administrative projects (design, planning, implementation, communication, etc.) Supervisory tasks: • Act as Mentor for temporary employees, apprentices or assume a limited project coordination/management role Minimum requirements What you’ll bring to the role: • Commercial training (e.g. Swiss Association of Commercial Employees, business school) or equivalent (e.g. other vocational qualification) • Fluent in English and German (written and spoken) is a must, knowledge of other languages (e.g. French) preferred • Experience as „Administrative Professional“ and additional career training is a must • Excellent organizational / administrative skills and experience Timing: As soon as possible – February 28, 2021 Please make sure to add a CV and Cover letter to your application. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitDivision ManagementLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaFacilities & AdministrationJob TypeFull TimeEmployment TypeTemporaryShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

20.02.2020

Novartis AG

Novartis Innovation Postdoctoral Fellowship, NIBR, Basel (Switzerland)

  • Novartis AG

  • 4040Basel

  • 20.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289991BRPosition TitleNovartis Innovation Postdoctoral Fellowship, NIBR, Basel (Switzerland)Apply to JobSourcing Statement You are applying to be part of the Novartis Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV. Job Description Are you a talented and passionate early-career scientist whose goal is to make innovative medicines? The Novartis Innovation Postdoctoral Fellowship offers aspiring drug hunters a unique opportunity to join our teams at the Novartis Institutes for BioMedical Research (NIBR), the innovation engine of Novartis. Mentored by experienced NIBR scientists, Innovation Fellows will gain first-hand experience in the design and development of breakthrough therapies and innovative technologies. We are looking for Innovation Fellows who will harness their scientific creativity and natural curiosity to help bring transformative treatments to patients. Join us as we reimagine medicine together. All applications will be evaluated by a review team comprised of NIBR discipline experts and candidates selected as finalists will be invited to our Basel (Switzerland) campus for an all-day interview in June 2020. New Innovation Fellows will start in September 2020 at our Basel site. Program highlights: • Program duration: 2-3 years • Mentorship & access to technology: Innovation Fellows will drive a multi-year research project under the mentorship of distinguished NIBR scientists and have access to NIBR state-of-the-art technology platforms to achieve their research goals • Curriculum: at the start of their Fellowship, Innovation Fellows will attend a comprehensive training series (boot camp), including dedicated courses covering the fundamentals of drug discovery and development as well as a communication skill workshop. • Short-term rotations: Innovation Fellows will participate in a tailored rotation schedule in both scientific and business-related disciplines to broaden their exposure and skillset • Fireside chats with local leading scientists and entrepreneurs • Community: Innovation Fellows will join our vibrant postdoctoral community for dedicated events, including the monthly postdoctoral seminars and our annual Research Day Symposium Minimum requirements Qualifications • Early-career scientists (MD and/or PhD), with terminal degree received within the last 3 years (students graduating in the next 5 months are eligible to apply) • Dedicated to translating scientific discoveries into medicines that improve human health • All scientific and technical disciplines welcome (biology, chemical biology, chemistry, computational and data sciences, and more) • Strong publication record or other scientific achievements (i.e. awards, patents) • Entrepreneurial mindset and boundless curiosity Please submit your CV and cover letter by April 24, 2020 for consideration. Include a potential area of unmet medical need where you believe you could make an impact. If you have any questions, please contact us at [email protected] Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

20.02.2020

Novartis AG

Global Integrated Insights Director, Neuroscience (80-100% )

  • Novartis AG

  • 4040Basel

  • 20.02.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID289933BRPosition TitleGlobal Integrated Insights Director, Neuroscience (80-100%*)Apply to Job Job Description 70-year history and sustained commitment in neuroscience, Novartis brought landmark therapies to patients with e.g. Multiple Sclerosis, Alzheimer’s disease, Parkinson’s Disease, Epilepsy, Depression and Migraine. We have a world class pipeline in neuro-inflammation, neurodegeneration, neuromuscular, pediatric neurology and refractory psychiatric diseases. The Integrated Insights Director is a leadership role, embedded within the franchises and serving as the main point of contact for market and stakeholders insights for the worldwide franchises across pipeline stages. The role identifies key business questions, leads the development and oversees the execution of an Integrated Insights Plan and its various components like Primary Market Research, Forecasting, Business Analytics and Competitive Intelligence in collaboration with top Country Pharma Organisations. The role proactively brings actionable Insights to the business and is accountable for collaboratively and challenging working with all stakeholders, with significant focus on ensuring tight alignment and informed decision making at Global Product Teams and country teams. Your responsibilities will include: • Enabling Franchise Leadership for our key therapeutic areas to make strategic decisions by bringing an external perspective and data based insights meanwhile applying industry leading primary and secondary market research approaches • Developing and implementing an Integrated Insights Plan for priority brands, disease areas and key markets, in line with the Franchise strategy • Promoting innovation and capability building, including new techniques, data sources, automation and artificial intelligence to enhance process efficiency and value of Insights • Providing proactive thought leadership and credibility in defining the strategy • Being a functional leader, that is able to influence across senior leaders in the worldwide and country franchise teams • Driving a mindset of Insights to Impact, leveraging actionable insights in decision making process [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#][#video#https://www.youtube.com/watch?v=ggbnzRY9z8w{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • University degree, ideally MBA or a professional qualification • Minimum 10 years of business insights (market research & analytics) experience in a global or multiple geography environment Global experience or multiple geographies • Ability to synthesize information to develop recommendations, and to persuade/influence senior stakeholders on a recommended path of action • Ability to translate complex reports and analysis into simple ‘business speak’ and present results to internal clients up to the executive level Business • Vendor assessment and management as well as experience Desirable requirements: • Neuroscience Therapeutic Area expertise • Scientific education would be beneficial Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

20.02.2020

Novartis AG

Global Head Trial Monitoring Portfolio Delivery Office

  • Novartis AG

  • 4051Basel

  • 20.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289221BRPosition TitleGlobal Head Trial Monitoring Portfolio Delivery OfficeApply to Job Job Description 350+ trials, about 25.000+ patients per year! You will have the oversight and project management of the global monitoring operational aspects of clinical trial execution across the entire Global Drug Development (GDD) portfolio. Our aspiration is to support the global Novartis development portfolio by recruiting patients for our clinical trials, ensuring that the right patient gets into the right trial in the right country. Your key responsibilities: Your responsibilities include, but are not limited to: • In alignment with the GDD strategy, develop long-term drug portfolio operational plans. Align with GDD stakeholders • Accountable to identify needs within Trial Monitoring (TMo) related to information and prioritization on drug portfolio and ensure processes and tools are in place to enable full alignment and transparency including portfolio outlooks and related risks and opportunities for TMO. • Identify synergies and potential competition within portfolio and align with other line functions to ensure efficient and effective delivery of objectives. • Drive and support implementation of initiatives at GDD and Global Development Operations (GDO) level to optimize execution of trials, including ongoing assessment and review of processes, systems and digital solutions. • Drive proactive risk management and contingency planning across TMO and communicate program status with the respective stakeholders in a transparent and timely manner. • Perform robust, independently documented TMO risk assessments on drug portfolio in partnership with Regional Heads, TMO Portfolio Delivery and other GDO line functions to identify root causes, and attain an aligned cross-functional risk status. • Define and maintain TMO portfolio objectives, prioritization and tracking, including identification of key portfolio issues and opportunities in alignment with GDD and GDO strategic priorities. • Lead teams to develop reporting methodologies and implement performance reporting for trials on monitoring deliverables (e.g. SIV, recruitment) in alignment with TMO Operations. Ensure consolidation, oversight and forecast accuracy of key trial milestones and KPIs at portfolio level. Provide regular updates and reporting to relevant GDD stakeholders (including but not limited to GDO Line functions, with ongoing review of portfolio strategy and prioritization for Trial Monitoring) [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Advanced degree or equivalent education/degree in life science/healthcare required • ≥12 years of pharmaceutical clinical drug development experience recommended (with 10 years minimum in planning/execution global clinical trials recommended) • Have led shaping strategy and translation of strategy into an operational risk management plan • Proven leadership and accomplishment in all aspects of conducting global clinical trials and programs and have had direct people management experience of 8 or more years. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. [Compliance sentences relevant to country] Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

20.02.2020

Novartis AG

Senior Legal Counsel, CRM Franchise

  • Novartis AG

  • 4051Basel

  • 20.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288330BRPosition TitleSenior Legal Counsel, CRM FranchiseApply to Job Job Description 125,000 unique individuals work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose: to Reimagine Medicine for millions of patients around the world. Come and join the team. Adopt an active approach in negotiating complex contracts independently. Substantiating recommendations allowing the Company to appreciate its contractual and statutory obligations, managing disputes and litigation, and assisting in management decision processes with robust risk assessments. Counsel and give strategic advice on product related matters for a global franchise enabling marketing, medical and strategic direction of the franchise portfolio, including legal support and strategic advice on alliance management matters, divestments and out-licensing transactions. • Lead lawyer responsibility for global licensing, co-promotion and other significant com-mercial agreements • Lead lawyer responsibility for global divestments and out-licensing transactions. • Manage local & regional responsibility for legal issues relating to key product(s) & thera-peutic area(s) in the Business Units and direct engagement with key clients • Act as business partner regarding contractual negotiations & statutory obligation activi-ties; in particular relating to the ownership, control and protection of inventions and con-fidential business information, including reviewing legal and business issues regarding the Company’s research and development collaborations and licensing activities relating to specific product(s) and therapeutic area(s) • Assist the company’s Alliance Management Team in resolving business issues in signifi-cant on-going third party relationships • Support legal positioning on public announcements and promotional material relating to specific products or alliances • Advise and determine appropriate actions regarding compliance issues, such as anti-trust, privacy and regulatory Minimum requirements • Law school graduate & Bar member • Fluency in English essential; knowledge of at least one other European language preferred. • 7 years minimum post Bar experience; ideally gained within a healthcare / pharmaceutical environment, or alternatively, with a top-tier law firm representing healthcare & technology clients. • Ability to analyze complex legal issues. • Strong verbal & written communication skills; together with a high ability to influence and negotiate. • Proven ability to deal positively when working within tight time pressures & demanding clients. • Strong experience in handling a high volume of activity involving multiple, often complex projects simultaneously. • Demonstrate professional & culturally sensitive work ethic WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGlobal LegalLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

19.02.2020

Novartis AG

Artificial Intelligence Internship - Real World Evidence Epidemiology

  • Novartis AG

  • 4051Basel

  • 19.02.2020

  • Praktikumsstelle

Back to Previous Page Job ID289845BRPosition TitleArtificial Intelligence Internship – Real World Evidence EpidemiologyApply to Job Job Description Artificial Intelligence (AI) a New Frontier in Algorithmic Medicine! In 2019 Novartis’s medicine reached 799 million patients in 150 countries across the world. The treatment guidelines are an essential part of treatment and this project aims to use Artificial Intelligence to synthesise evidence on all treatment regimens for the diseases that Novartis’s medicines are intending to be used. Evidence synthesis and algorithms are at the heart of evidence-based medicine and are part to determining the most appropriate, the best and the optimal medical interventions for patients. It involves a frequent and rapid assessment of the literature reporting the results of studies conducted involving the interventions. As an intern, you will be able to acquire the skills in clinical use of AI and machine learning in evidence synthesis for the practice of evidence based medicine. You will also get an opportunity to fine tune your skills in the development of machine learning algorithms and interactive visualization platforms. Your responsibilities: Your responsibilities include, but are not limited to: • Develop AI / Machine Learning algorithms and a toolkit for clinical phenotyping of the diseases of interest to Novartis using patient level data in combination with wider summary level (study level) data • Testing and further develop the state of art machine learning algorithms in the area known as “word embedding’s” (and possibly others) relevant to the clinical embedding space. The toolkit will comprise of the algorithms, and an interactive visualization platform forming into a Disease Evidence Portal to be used by the global medical and scientific community within Novartis Minimum requirements What you’ll bring to the role: • Currently enrolled in an accredited university or recently graduated (BSc and MSc), in AI, computer Science, Machine Learning and/or data science/engineering • Good programming skills in Python/R with open sourced machine learning toolkits and R/Shiny toolkit for developing interactive dash boards • Fluent in English (spoken and written), additional languages will also be useful • Experience or passion for learning more about Disease Epidemiology, Disease Outcomes, and quantitative / statistical assessment of treatment outcomes Duration: The internship is for the duration of 3-6 months. (April –October period) Please apply with your CV and a cover letter illustrating your motivation to get involved in such an activity Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionPHARMABusiness UnitGLOBAL MEDICAL AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

19.02.2020

Novartis AG

Postgraduate in Biologics Development for Upstream Process Intensifica

  • Novartis AG

  • 4040Basel

  • 19.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID284060BRPosition TitlePostgraduate in Biologics Development for Upstream Process IntensificaApply to Job Job Description 36! That’s the number of exploratory new biological entities we are developing to improve and extend people’s lives. In order to advance this diverse pipeline of biopharmaceutical products we are looking for a postgraduate scientist in the field of cell culture process development to support the improvement and intensification of cell culture processes as well as the exploration of new technologies for therapeutic protein manufacture. Your responsibilities: Your responsibilities include, but are not limited to: • Support the development of efficient, high-yield, robust and scalable fermentation processes for new biological entities • Support the improvement and intensification of established fed-batch cell culture processes from vial break to harvest, including seed and main bioreactor stages • Support the implementation and evolution of (semi-)continuous perfusion cell culture processes • Support the evaluation and implementation of new equipment and technologies in the USP environment • Work in multidisciplinary and international teams and at the interfaces to related drug substance process development and analytical functions Minimum requirements What you’ll bring to the role: • Master of Science in Life Sciences in e.g. Biotechnology, Biochemistry or Bioengineering with basic knowledge in upstream processing or equivalent education/experience • Practical experience with mammalian cell cultures • Basic laboratory experience with cell cultures, primarily aseptic handling, ideally with shake flasks, wave and stirred bioreactors • Intrinsic curiosity, willingness to adopt challenging tasks and grow in related areas of expertise (e.g. parallelized, automated fermentation) • Proficiency in English, oral & written. Proficiency in German would be an additional asset Please apply with your CV and a cover letter mentioning your availability for this position. Duration: Starting immediately, for 12 months Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternship Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

19.02.2020

Novartis AG

Postdoctoral Scholar

  • Novartis AG

  • 4040Basel

  • 19.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288700BRPosition TitlePostdoctoral ScholarApply to Job Job Description Postdoctoral scholar – Computational Sciences, Chemistry NIBR The Novartis Institutes for BioMedical Research (NIBR) is the innovation engine of Novartis. We collaborate across scientific and organizational boundaries, with a focus on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. An exciting opportunity is available to do research at the interface between Computer-Aided Drug Discovery (CADD), Cheminformatics and Research Informatics. Among our groups, we help project teams to use the right data at the right time to take the best decisions to optimize small molecule compounds against multiple objectives. Our cross-departmental structure of experts from different fields is set up to find novel methods to automatically extract, analyze, and understand those decisions from historical data. Leveraging on recent advances in the fields of machine learning and behavioral analysis the derivation of those decision patterns taking into account biological (assay data) as well as chemical (reactions, building blocks) information has become a true possibility. For this, we seek an enthusiastic postdoctoral researcher with a focus in statistics, computational or data science and preferably knowledge in cheminformatics (https://www.novartis.com/our-science/postdoc-program/research-themes/chemistry/nikolaus-stiefl-phd). The successful candidate will join a vibrant scientific community and collaborate with other postdoctoral fellows mentored by a range of scientists across disciplines and platforms, including chemistry, structural biology, molecular biology, functional genomics, neurophysiology and translational medicine. Postdoctoral scholars at NIBR have a unique opportunity to conduct innovative, interdisciplinary research and are expected to publish their results in leading journals. The postdoctoral term is up to 4 years. Minimum requirements Qualifications: - PhD in natural or technical sciences with a focus on computational and/or statistical approaches. Chemistry knowledge is a strong plus (PhD students in the last year of their thesis work, are also eligible to apply). - Additional qualifications - Hands-on experience with general machine learning libraries - Programming skills (software development experience is a plus) - Strong publication record - Excellent analytical, communication and organizational skills - Candidates must be able to work independently as well as with interdisciplinary teams Please submit your cover letter and CV, including the contact information (name, institution, phone number, and e-mail address) of 3 references. For more information about our postdoctoral program, please visit https://www.novartis.com/our-science/postdoc-program Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. Novartis is an equal opportunity employer committed to embracing and leveraging diverse backgrounds. M/F/D/V.DivisionNIBRBusiness UnitGlobal Discovery ChemistryLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

19.02.2020

Novartis AG

Head of Scientific Products - Information Products and Data Sciences

  • Novartis AG

  • 4051Basel

  • 19.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID284546BRPosition TitleHead of Scientific Products - Information Products and Data SciencesApply to Job Job Description 6,000 scientists and physicians around the world use our data reimagine medicine and create therapies that save lives. You can multiply the value and impact of these data for Novartis scientists. Our research is focused on discovering innovative new drugs that will change the practice of medicine. Novartis Institutes for BioMedical (NIBR) is the global pharmaceutical research organization of Novartis. We have an open and entrepreneurial culture, encouraging collaboration to make effective therapies. At NIBR, our mission is to discover innovative medicines that treat disease and human health. To do that, our scientists need cutting-edge, state-of-the-art computing systems. With NIBR Informatics (NX), NIBR is making a strategic investment into informatics capabilities and is positioning itself to deliver the systems and services that are critical to the future of drug discovery. The Information Products and Data Sciences (IPDS) group in NX is driven to maximize the impact and value to NIBR of software and data. We deliver powerful, functional, beautiful, and integrated software solutions that create a frictionless user experience. Our organization is here to build and apply excellence in product and data management to further Novartis drug discovery. Job Description: As the Head of Scientific Products, you will develop and continually update a vision for the suite of scientific products that support NIBR drug discovery and lead the product management team to the successful realization of that vision. Your vision will inspire the cross-functional product organization to deliver value to our scientists and will sustain our team through challenging times. You will bring together technologies, capabilities and outstanding talent to create products that our users will love. You will define the standard for excellence in product management in our organization and synthesize that with your knowledge of drug discovery to create scientific software that enhances and helps drive NIBR science. The Head of Scientific Products will prioritize product roadmaps, direct development resources to maximize value to NIBR science, and will define how we measure product success and value delivery. You will be responsible for identifying opportunities that lead to the growth of our products through constant improvement and innovation while also providing consistent delivery and stable operation of products. You will use your knowledge of these products to promote their meaningful use by giving product demos, sharing user stories, and showing the connection of our scientific products to drug discovery impact. You will work closely with colleagues in engineering, user research, design, support, training, and data science to empower matrixed product teams that deliver on your vision for our products. This will require you to align and coordinate with other departmental leaders and stakeholders to ensure all operational needs are met including security, stability, usability, and sustainability. Responsibilities include but are not limited to: •Lead, manage and mentor a team of product managers. •Product lifecycle management from concept to launch of the products across all scientific product lines. •Lead, define, represent and communicate product portfolio strategy to all stakeholders and NIBR leadership. •Assess product development progress and enhancement opportunities. •Evaluate product development results. •Evaluate and provide input into strategic plans for each product line. •Drive innovative ideas, solutions and products through leadership and decisive action. •Build incredible teams and processes to deliver products that satisfy the needs of customers. •Become the key evangelist of our products and participate in education activities, conferences, discussions with thought leaders within and outside of Novartis. •Regularly present to stakeholders, NX, and NIBR leadership Minimum requirements What you will bring to this role: •Bachelor’s degree in biology, chemistry, computational biology or computational chemistry (PhD preferred) •Minimum of 10 years of experience in product management in complex matrix environments •Five or more years of work experience in drug discovery or a core supporting scientific discipline such as biology, chemistry, or computational sciences •Experience with Agile software development •Strong quantitative skills and the ability to use data and metrics to inform decisions Additional required core skills: •Outstanding interpersonal and communication skills; adept at working with colleagues from diverse disciplines and at all levels of the company. •Proven experience in team building, mentoring, and leadership •Demonstrated strength as a team player •Strong leadership skills with a proven ability to win others to follow a common vision •A clear and visible set values and demonstrated integrity •Proven ability to execute consistently, rapidly, and effectively •Self-motivated •Calm under pressure •Ability to travel 25% Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Trial Monitor Senior Process Control Manager

  • Novartis AG

  • 4051Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID274708BRPosition TitleTrial Monitor Senior Process Control ManagerApply to Job Job Description 46’000! That is the number of patients in clinical trials at Novartis. The Trial Monitoring organization (TMO) drives execution of clinical trials in countries ensuring highest quality monitoring at sites. Our organization extends monitoring services to Global Drug Development (GDD), Novartis Institutes for Biomedical Research (NIBR), and to Global Medical Affairs (GMA), with operations in 56 countries, monitoring ~540 trials, ~21’140 sites and more than 46’000 patients. As Senior Process Control Manager, you will be accountable for leading global quality process improvement and compliance activities, and for oversight and control of quality in the Trial Monitoring Organization. You will work collaboratively with Clinical Quality Assurance to ensure improvement of quality and completion of risk management activities. Your responsibilities will include: • Metrics and Quality KPI – Leads the tracking and reporting of compliance to the established clinical monitoring processes. Responsible to analyze, track, report and reinforce adherence to applicable performance measures. Oversees and recommends corrective actions based upon report outputs; ensures that training is developed and implemented as applicable to redirect teams to better Quality KPI scores. Tracks audit and inspection findings, report on results, track trends, generate lessons learned. Ensures effective ongoing operations of the Risk Mitigation Assessment process to improve the rate of compliance of countries to TMO quality standards. • Process Expertise – serves as subject matter expert and input into new SOPs on behalf of TMO, ensures compliance to and adequate training opportunities for new SOPs and Business Guidance. Serves as deputy for the Process Control Global Head in Trial Monitoring. Serves as Lead SME on the monitoring processes as requested. Ensures the alignment of TMO and other monitoring groups to create the most effective and compliant process improvements. Tracks deviations from Monitoring SOPs and ensure appropriate documentation is filed, and corrective actions are taken. Identifies procedural gaps and drives correction with process improvements where applicable. • Process Compliance – Ensures CAPA commitments are adequate, submitted and completed in a timely manner. Ensures audits and inspections are supported and tracked, and outcomes requiring corrective action are managed. Reviews CAPAs and makes appropriate recommendations to keep consistent actions across TMO. Initiates and documents root cause investigations of critical issues in collaboration with Quality Assurance and Clinical Operations. Supports the generation and dissemination of Tactical Memos and Lessons Learned communication in collaboration with monitoring training. Leads the conduct of Trial Master File quality control checks. Ensures TMO compliance with required training by tracking and reporting compliance status for the Global, Regional and Country level organizations. Identifies gaps and assign action where needed to promptly gain compliance. Minimum requirements What you’ll bring to the role: • College or University degree with significant life science experience. Advanced degree in life sciences preferred. • A minimum of 8 years in a R&D regulated environment in a relevant pharmaceutical or health care company, desirable clinical operations experience • Extensive knowledge and experience in ICH-GCP Process Control or ICH-GCP Quality Assurance systems and Health Authority regulations; Clinical Operations experience in these areas is preferred • Demonstrated ability for leading initiatives with cross-functional teams and implementation of recommendations • Experience working in matrix environment and in global teams WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Storage, Backup and Data Transfers Service Manager

  • Novartis AG

  • 4051Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289582BRPosition TitleStorage, Backup and Data Transfers Service ManagerApply to Job Job Description 6,000 scientists and physicians around the world use our data & systems to reimagine medicine and create therapies that save lives. At NIBR, our mission is to discover innovative medicines that treat disease and human health. To do that, our scientists need cutting-edge, state-of-the-art computing systems. In this role as the Storage, Backup and Data Transfers Service Manager you will be apart the Infrastructure Services group in TUS which is accountable for the full lifecycle of multiple infrastructure services within their domain. As the Service Manager your role is essential within NIBR’s journey toward a culture of Service Excellence. Responsibilities include but are not limited to: •Creation, maintenance, and evolution of roadmap and vision •Definition of Service Excellence and associated Service Level Objectives (SLOs) •Capacity planning, budget forecasting and tracking • Driving a matrixed team towards stable, reliable and performant delivery of services in the area of responsibility •Definition, periodic review and follow-up of metrics relevant to the service domain •Proven ability to indirectly influence resources and decision makers across organizational boundaries in a large enterprise •Ability to interact with user communities of varying degrees of expertise and understand their requirements • Ability to leverage existing relationships and develop new connections through exceptional interpersonal skills as well as communicates effectively, is structured, precise and reliable in their work •Tackles ambiguity and collaborates with others to address uncertainty with the ability to thrive in a dynamic, matrixed operating model •Technical knowledge in one or more of the following technical areas is advantageous On-premise storage: EMC Isilon, EMC ECS / CloudPools, NetApp FAS / OnTap Cloud storage: AWS S3, AWS Glacier Backup: Cohesity, NetBackup Data transfers: Aspera [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] NIBR is making a strategic investment into informatics capabilities and is positioning itself to deliver the systems and services that are critical to the future of drug discovery. You can enable our NIBR Informatics group (NX) realize its highest value through a fully integrated portfolio. Within NX, the NOE department is responsible for helping NX delivers the highest value within a reasonable cost. NOE is responsible for central management of NX’s budget and ensures that NX delivers on financial goals. It helps NX to define its single strategy and realize it through fully integrated portfolio. NOE supports product and service delivery through disciplined planning, delivery, monitoring and measurement of results. Minimum requirements What you will bring to this role: •University degree in IT or related field, or equivalent work experience. •Minimum of 3 years of progressive experience that combines both business and technology realms •Exceptional relational skills and stakeholder management; ability to influence at all levels of the organization and a team player •ITIL Foundation (V3 or V4) certification is preferable •Past experience in an IT service management role, providing services within or to large organizations, is a plus •Well-developed influencing skills with a proven ability to bring folks together and drive alignment •Ability to travel up to 10% Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Data Scientist / Machine Learning Expert

  • Novartis AG

  • 4051Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288092BRPosition TitleData Scientist / Machine Learning ExpertApply to Job Job Description 125,000 unique individuals work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose: to Reimagine Medicine for millions of patients around the world. Come and join the team. We are seeking a unique data scientist with the skills, experience and passion to extract new knowledge and disruptive insights from the large and rich body of data collected by one of the world’s leading pharmaceutical companies. You will be a member of our global Computer-Aided Drug Discovery (CADD) group, an interdisciplinary team of expert molecular modelers, cheminformaticians, and data scientists. Teamed up with domain experts from biology, chemistry and translational medicine, this is a unique opportunity to develop and apply cutting-edge machine learning technologies to uncover insights to real-world drug discovery problems and innovate paths to new medicines. • Develop and implement methods for extracting patterns and correlations from both internal and external data sources using machine learning toolkits • Develop workflows for conducting comparative analysis among Novartis’ diverse data sources as well as generalizing approaches developed in-house or externally. • Enable open-source solutions for internal use and implement cutting-edge published scientific methods. • Develop customized machine learning solutions including data querying and knowledge extraction. • Interact and be part of interdisciplinary project teams to drive effective decision-making by mining and developing predictive models • Develop new skills in the area of cheminformatics and drug discovery and leverage those to accelerate development of new machine learning algorithms • Keep ahead of scientific literature and interact with internal and external scientists to integrate novel data science technologies Minimum requirements • Advanced degree (M.Sc. or higher) in data science and machine learning, statistics, computer sciences, cheminformatics, mathematics, computational chemistry, computational biology, bioinformatics, or English and German • In-depth experience with modern and classical machine learning methods • Strong statistical foundation with broad knowledge of supervised and unsupervised techniques • Programming experience (preferred Python, R, C++) preferably in Linux and high-performance computing environments • Good listener - strong, concise, and consistent written and oral communication • Talent for communicating stories through data visualizations • Proven ability to collaborate and co-develop solutions with others • A passion for tackling challenging problems and developing creative solutions • A drive for self-development with a focus on scientific know-how WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitGlobal Discovery ChemistryLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Global Program Clinical Head - retina

  • Novartis AG

  • 4051Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID281046BRPosition TitleGlobal Program Clinical Head - retinaApply to Job Job Description One mission! to deliver innovative medicines to the millions of patients worldwide who live with eye diseases In your role, you will be the global leader of the clinical development team who is responsible for a clinical program with a compound being developed in one or more treatment indications. You will be accountable as leader of the Global Clinical Team for design, implementation, execution, and submission/approval of a clinical development plan to support decision milestones, regulatory requirements, and budget targets. Your responsibilities will include: • Lead the Global Clinical Team (GCT); clinical development representative at the Global Program Team (GPT) • Lead the development and execution of the Clinical Development Plan (CDP), adhering to Novartis clinical/data standards for Phase II – III trials designed for successful global registration of the compound. Ensure individual protocols are consistent with CDP and are aligned to achieved the Target Product Profile (TPP) • Lead creation of clinical components of key documents (regulatory documents, registration dossiers, value dossiers, pharmacoeconomic dossiers) supporting registration, market access, and commercialization of the compound(s) • Support the Clinical Science Unit/CSU Head, driving excellence in clinical trial strategy, design, and execution. This includes CDP, Executable Synopsis (ES), protocol reviews, and development of disease/program clinical standards. By working as part of the CSU, lead clinical interactions with external and internal stakeholder and support NIBR/Translational Sciences especially in driving transition of pre-PoC projects to DDP and BD&L including target identification and due diligences together with other medical matters as needed • Act as medical expert and leader in interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal stakeholders (e.g., Research, Translational Sciences, Global Medical Affairs, Marketing, HE&OR), and internal decision boards • Responsible for continuous evaluation of drug safety profile, including the aspects of relevance to patients in clinical studies, as well as external stake holders (e.g., health authorities) with support from Drug Safety & Epidemiology • Ensure compliance and adherence to clinical quality initiatives and plans • Ensure quality of all clinical documents (e.g., Investigators’ Brochure, protocol, study report, clinical components of regulatory submissions, safety related documents) produced by Global Clinical Team (GCT) • Deliver all relevant components/documents for maintenance of product licenses (e.g., Core Data Sheet generation/revision; clinical benefit-risk assessments for license renewals, responses to Health Authority) Minimum requirements What you’ll bring to the role: • MD or equivalent required. Advanced knowledge in ophthalmology required • Development in an academic or industry environment spanning clinical activities in Phases I through III (some industry experience preferred) • ≥ 5 years of demonstrated leadership, management, and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical or biotech industry • ≥ 5 years people management experience required, this may include management in a matrix environment (direct report management experience preferred). Global people management experience desirable • Demonstrated experience in data presentation • Strong negotiation and diplomatic skills, experience with health authorities required relationship of departments, business priorities), WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Global Product Owner xDROID

  • Novartis AG

  • 4040Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288562BRPosition TitleGlobal Product Owner xDROIDApply to Job Job Description 30,000+ associates in Pharma and Oncology are focused on getting our medicines to the patients that need them while providing value added services to Healthcare Providers. Our Digital Commercial Execution team has been formed to provide digital programs and solutions at scale that will have significant impact on the success of the enterprise and that are implemented at scale across our Pharma and Oncology businesses. These solutions are relevant to millions of customers and applicable to more than 100,000 daily interactions with Healthcare Providers. Play a key role in a team that will build an industry leading, future-proofed foundation that will power commercial teams by putting data, digital, and artificial intelligence in practice. In this role you are responsible for defining and creating a digital product as part of an industry-leading commercial data analytics platform for Pharma and Oncology that will improve the impact of our sales and marketing teams. You will support our commercial business units to move from data rich to delivering insights from data/digital to benefit our patients. You will lead a Product Team working to deliver the xDROID omnichannel vision for the company for a significant customer group (e.g. Sales, Marketing, Medical, or Access, etc) with campaign content optimization and automation for better personalization of campaigns and more efficient asset utilization. The Product Owner sets the product vision, identifies, and prioritizes features to build a minimum viable (lovable) product to incrementally deliver maximum business value. You are accountable for maximizing the value and use of a product, as measured by business KPIs, throughout the product lifecycle. The Product Owner is a servant leader to an empowered team and responsible for being empathetic to the customer and making decisions based on the customers’ needs. Your responsibilities will include: Serving the customer: • Ensure the customer’s needs are driving the design of the product throughout the product lifecycle • Maintain ongoing interaction with the customer, including through demos and pilots, ensuring customer’s needs are understood and fulfilled in the product • Measure and respond to customer input, experience, and feedback to ensure high satisfaction with the product • Ensure deployment success by partnering with the business to successfully implement tools and support business to evolve relevant business process End-to-end product accountability • Drive product definition, set clear vision, and roadmap, continuously communicating it Supporting empowered Product Teams: • Accountable for the product’s output and value of the product • Ensure the team is comprised of the necessary skillset and capabilities to deliver the product • Establish and manage teams of individuals with diverse backgrounds Stakeholder engagement and communication: • Work with stakeholders within the organization to build transparency and incorporate inputs as needed • Ensure ongoing awareness and alignment between product team and partners • Champion product vision, secure resources and remove roadblocks [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Technical/ Scientific degree level qualification (Pharmacy, Engineer, Chemistry); professional accreditation in Data Science and/or enabling technologies desired • Proven Product Management skills; experience working in product teams or innovation or startups or digital/tech highly desirable • Experience working on technical or analytical projects, with a deep understanding of customers • Experience working in a complex organization, building relationships and driving engagement • A toolkit for product leadership that includes an understanding of Agile and Lean methodologies, and OKRs. Experience of delivery through these methods is highly desirable • Commercial experience in various roles and within pharma highly desirable • Ability to drive with limited information, willingness to adapt, speak-up and challenge, and take calculated risks • Intense curiosity: able to dig beneath the surface of a problem, interrogate the question, and synthesize clear hypotheses that can be engineered and tested. • Empathy with customers and ability to understand being in their shoes; obsessed about impact • Openness to new ideas and alternative perspectives; able to adjust and flex as needed to the customer • Previous experience and strong mindset in continuous improvement and change management; Excellent interpersonal and communication skills. • Ability to work independently and reliably. Experience in international, complex and dynamic environments. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitDIGITAL OFFICELocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Project & Program Management Lead, NIBR Informatics

  • Novartis AG

  • 4040Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289581BRPosition TitleProject & Program Management Lead, NIBR InformaticsApply to Job Job Description 6,000 scientists and physicians around the world use our data & systems to reimagine medicine and create therapies that save lives. At NIBR, our mission is to discover innovative medicines that treat disease and human health. To do that, our scientists need cutting-edge, state-of-the-art computing systems. In this role as the lead for Project and Program Management you will be accountable for providing a high level of expertise in Project and Program management and aligning Project and Program management skills with the Novartis Institutes for BioMedical Research Informatics (NX) delivery approach, values and culture. You will work side-by-side with Product Management and Engineering leads to identify the best approach for management of delivery and staff Product lines and Product teams with the right talent. Responsibilities include but are a not limited to: •Partner in execution of delivery across Products lines, Products and Projects, planning execution, managing delivery, identifying blockers and supporting teams •Help to plan complex activities and inter-dependencies across the Portfolio, contributing to commitment with confidence •Work with the Strategy and Portfolio management team to improve Portfolio level planning based on prior results •Understand full NX Portfolio, status of activities, issues and blockers, and deploy talent based on the priorities of the NX Portfolio •Collaborate with the entire NX Delivery Excellence team to integrate and advance best practice in Project Management in the context of Product and Service delivery •Early adopter of metrics/ methods of Service and Product Delivery, providing active feedback and steering methods to simplicity and impact •Collaborative leader practicing excellence in their field working across NX and with NIBR stakeholders; highly respected by broad NX community •Servant leader, supporting and coaching your team to success [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you will bring to this role: •Bachelor degree or higher in Technology, Life Sciences, or closely related subject •Formal Project and Program Management training (e.g. PMP) •Minimum 5 years of experience managing technology implementation projects (IT infrastructure, Software solutions and/ or Products) and programs with a complex Stakeholder landscape •Results-focus and passion for disciplined delivery •Excellent executive communication and influencing ability •Understanding of and experience working with key success drivers, constraints and complexities within a global organization (multi-site, multi-country, x,000+ employees) •Record of successfully implementing, operating and improving operational processes •People manager experience; a highly resourceful and motivated leader with a strong collaborative spirit •Proven track record of successfully using agile and adaptive project management approaches •Ability to travel 25% Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Global Product Owner ACTalya

  • Novartis AG

  • 4040Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288564BRPosition TitleGlobal Product Owner ACTalyaApply to Job Job Description 30,000+ associates in Pharma and Oncology are focused on getting our medicines to the patients that need them while providing value added services to Healthcare Providers. Our Digital Commercial Execution team has been formed to provide digital programs and solutions at scale that will have significant impact on the success of the enterprise and that are implemented at scale across our Pharma and Oncology businesses. These solutions are relevant to millions of customers and applicable to more than 100,000 daily interactions with Healthcare Providers. Play a key role in a team that will build an industry leading, future-proofed foundation that will power commercial teams by putting data, digital, and artificial intelligence in practice. In this role you are responsible for defining and creating a digital product as part of an industry-leading commercial data analytics platform for Pharma and Oncology that will improve the impact of our sales and marketing teams. You will support our commercial business units to move from data rich to delivering insights from data/digital to benefit our patients. You will lead a Product Team working to co-design with the end customer and further evolve the real time personalized AI assistant ACTalya for all field associates and ensure the solution meets the business needs as well as drives impact (productivity, sales, ROI...), integrating all other field tools to enable a single interaction and best end user experience. The Global Product Owner sets the product vision, identifies, and prioritizes features to build a minimum viable (lovable) product to incrementally deliver maximum business value. You are accountable for maximizing the value and use of a product, as measured by business KPIs, throughout the product lifecycle. The Product Owner is a servant leader to an empowered team and responsible for being empathetic to the customer and making decisions based on the customers’ needs. Your responsibilities will include: Serving the customer: • Ensure the customer’s needs are driving the design of the product throughout the product lifecycle • Maintain ongoing interaction with the customer, including through demos and pilots, ensuring customer’s needs are understood and fulfilled in the product • Measure and respond to customer input, experience, and feedback to ensure high satisfaction with the product • Ensure deployment success by partnering with the business to successfully implement tools and support business to evolve relevant business process End-to-end product accountability • Drive product definition, set clear vision, and roadmap, continuously communicating it Supporting empowered Product Teams: • Accountable for the product’s output and value of the product • Ensure the team is comprised of the necessary skillset and capabilities to deliver the product • Establish and manage teams of individuals with diverse backgrounds Stakeholder engagement and communication: • Work with stakeholders within the organization to build transparency and incorporate inputs as needed • Ensure ongoing awareness and alignment between product team and partners • Champion product vision, secure resources and remove roadblocks [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Technical/ Scientific degree level qualification (Pharmacy, Engineer, Chemistry); professional accreditation in Data Science and/or enabling technologies desired • Proven Product Management skills; experience working in product teams or innovation or startups or digital/tech highly desirable • Experience working on technical or analytical projects, with a deep understanding of customers • Experience working in a complex organization, building relationships and driving engagement • A toolkit for product leadership that includes an understanding of Agile and Lean methodologies, and OKRs. Experience of delivery through these methods is highly desirable • Commercial experience in various roles and within pharma highly desirable • Previous experience in continuous improvement and change management; excellent interpersonal and communication skills. • Ability to drive with limited information, willingness to adapt, speak-up and challenge, and take calculated risks • Intense curiosity: able to dig beneath the surface of a problem, interrogate the question, and synthesize clear hypotheses that can be engineered and tested. • Empathy with customers and ability to understand being in their shoes; obsessed about impact • Openness to new ideas and alternative perspectives; able to adjust and flex as needed to the customer • Previous experience and strong mindset in continuous improvement and change management; Excellent interpersonal and communication skills. • Ability to work independently and reliably. Experience in international, complex and dynamic environments. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitDIGITAL OFFICELocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Associate Director Biostatistics

  • Novartis AG

  • 4040Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID287196BRPosition TitleAssociate Director BiostatisticsApply to Job Job Description 200+ compounds in Novartis are supported by biostatisticians in 10+ sites around the globe. Biostatisticians transform clinical data into analyses that build the basis for making innovative drugs accessible for patients. They influence decision-making in cross-functional international teams from early to late phase drug development. As Associate Director Biostatistics, you will influence and drive statistical strategy and innovation through cross-functional collaboration and decision making for assigned trials/programs within (pre/ early/full) clinical development and/or medical affairs. You will demonstrate high levels of independence in support of complex clinical trials or low to mid complexity programs you will be responsible for leading quantitative strategy through collaboration with quantitative partners across the organization. Further, you will represent the Biostatistics and Pharmacometrics function at internal and external decision boards, develop and mentor other statisticians, and provide strategic, technical, operational and scientific leadership and solutions to the organization. You may serve as a manager of a small team. Your responsibilities will include: • Responsible for all statistical tasks on assigned clinical or non-clinical trials, and perform these tasks for high complexity trials with a high level of independence seeking peer input/review as required. Responsible for protocol development in alignment with the development plan, developing statistical analysis plan, and reporting activities • Contribute to planning and execution of exploratory analyses, innovative analyses related to publications and pricing & reimbursement submission and/or PK, PK/PD analyses, exploratory biomarker and diagnostic analyses, and statistical consultation. Initiate, drive and implement novel methods and innovative trial designs and dose-finding strategies in alignment with the Lead Statistician. • Provide statistical expertise to support submission activities and documents, meetings with and responses to Health Authorities, pricing agencies and other drug development activities, as required. • Independently lead interactions with external review boards/ethics committees, external consultants and other external parties with oversight as appropriate. Represent Novartis in statistical discussions at external congresses, conferences, scientific meetings. • Collaborate with other line functions. Explain statistical concepts in an easily understandable way to non-statisticians and provide adequate statistical justifications and interpretation of analysis results for actions/decisions/statements, when required. [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • MS (in Statistics or equivalent) with 10+ years relevant work experience or PhD (in Statistics or equivalent) with 6+ years relevant work experience • Strong interpersonal and communication skills bridging scientific and business needs • Effective utilization of innovative statistics and quantitative analytics to influence assigned program team decisions and support department to deliver objectives • Proven knowledge and expertise in statistics and its application to clinical trials. • Demonstrated excellence in use of statistical software packages (e.g. SAS, R). • Strong knowledge of drug development and Health Authority guidelines. • Experience independently leading a multidisciplinary team to achieve team objectives. • Strong understanding of Disease/Therapeutic Area and or regulatory activities. Expert scientific lead WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Post-doctoral Candidate

  • Novartis AG

  • 4040Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289622BRPosition TitlePost-doctoral CandidateApply to Job Job Description 4! Four areas in global health and global drug development we are focusing on to make a difference in people’s lives. Your work will be important in helping more people understand our incredible commitment to bring transformative medicines to more people worldwide. This position is open in the context of a Novartis Innovation initiative to support novel cross-functional programs. The work assignment will debut with developing extended release protein formulations for parenteral application and subsequently characterizing those delivery systems in vitro. We are looking for a highly motivated postdoctoral scientist with a passion for drug development. The candidate will demonstrate experience in executing laboratory experiments and applying technical knowledge aiming at the development of protein formulations and analytical methods. The role offers broad exposure to state of the art technologies in formulation, process optimization up to pilot scale as well as the establishment/adaptation of analytical methods. The research project will be performed in the Pharmaceutical Development department for parenteral dosage forms at the Novartis Basel Headquarter in collaboration with other departments, including the Center of Excellence for Spray-Drying. Minimum requirements - Ph.D. in Pharmaceutical Technology, or related fields in natural sciences with experience in formulation and analytical development of protein therapeutics and ideally parenteral extended release formulations. - Experience in spray drying is advantageous. - Due to the highly interdisciplinary project scope, a strong collaborative spirit. - excellent organization and communication skills are required. - English mandatory, German desirable. - Ph.D. thesis at University. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Global Senior OD Leader

  • Novartis AG

  • 4040Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289632BRPosition TitleGlobal Senior OD LeaderApply to Job Job Description 1 company – that is the journey Novartis is on in its quest to extend and improve people’s lives through reimagining medicine. We have a clear strategy: to be a focused medicines company powered by advanced therapy platforms and data science. We recognise our people drive our company and significant effort is being invested in unleashing their power through the transformation of our culture and our organisation. A number of significant changes are underway in our company with incredible energy from our top leaders. We are looking for an experienced organisation development consultant who will partner with our leaders to grow the impact of this important work. Position Purpose Partner business leaders and PO colleagues to diagnose and address complex enterprise-wide organisational challenges that cut across Novartis’ business, using deep Organisation Development and Change (OD) experience and support the development of OD capability across the company, which enables Novartis to successfully and sustainably drive its transformation, contributing to the mission of reimagining medicine to improve and extend people’s lives. Major Accountabilities • This role is a senior expert position with primary focus to diagnose and address complex organisational challenges at the Enterprise level that cut across Novartis businesses. • The role holder should work in an integrated and collaborative way with business leaders and their teams and PO and other functional colleagues. Collectively, these teams address business and organisational challenges and opportunities in light of Novartis strategy and create the organizational capability needed to drive business performance. o On occasion, support may also be given to OD requirements within specific divisions on request of business TMOD colleagues. • Specifically, the OD Advisor role should: o Support diagnosis of complex organisational challenges and opportunities at the Enterprise level o Deliver top quality organization design, development and change management advice and interventions in line with diagnosis done • Actively contribute to the collective capability development of OD as an active member of the OD and PO community in support of business needs, through: o Leading the development and implementation of high quality enterprise-wide OD approaches in support of identified business needs in partnership with colleagues in the OD community for use across the company o Sharing knowledge and experience gained from OD interventions o Working closely with PO colleagues participating in delivery of OD and change activities o Contributing to skills development activities in the OD area o Providing thought leadership in line with expertise Minimum requirements Minimum requirements : Education: Relevant degree, postgraduate and working qualifications preferred in the relevant business or applied behavioural sciences (e.g. Strategy, Business Administration, Organization Development, Psychology, HRM, MBB, etc). Languages: Fluent in English Experience: Significant OD experience, supported by broader consulting, PO or change management experience. • Strong experience with senior executive engagement and facilitation, strong influencing ability through consulting, communication and relationship building skills • Proven analytical and conceptual skills, combined with ability to implement • Proven expertise in OD and change management methodologies and (successful) global project delivery • Known for strong collaboration and networking with the broader PO community and other stakeholders • External consulting and/or business leadership experience would be valuable WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitGROUP HUMAN RESOURCESLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaHuman ResourcesJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Novartis Digital Recruitment Digital Media Lead

  • Novartis AG

  • 4040Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288272BRPosition TitleNovartis Digital Recruitment Digital Media LeadApply to Job Job Description 600 clinical trials! Novartis runs nearly double the number of clinical trials of any other pharmaceutical company. We have an unparalleled need for patients - at least 25,000 patients every year. Over 70% of those trials are late – mostly because we can’t find enough patients. But at the same time, 85% of patients say that they don’t know what their options are to participate in a clinical trial. This is a travesty – for Novartis and the patients who are waiting for our medicines or are looking for ways to contribute to helping those afflicted by disease. Come help us solve this problem using data, digital and social media – you can be instrumental in bringing hope and making an impact for patients. Position purpose: The Novartis Digital Recruitment Digital Media Lead is accountable for delivering recruiting funnel performance by creating the channel strategy, in concert with the digital recruiting strategist, managing placement and optimization in real time. This role be responsible to experiment with different channel placements, optimize for maximal ROI, and extract learnings relevant for recruiting purposes. This is an enterprise role whose scope will span studies in GDD, NIBR, Pharma, Oncology and GMA with a high requirement to collaborate and find win/win strategies across other efforts. The role will have Global responsibilities, though initial focus for first ~6-8 mo will be US. Major responsibilities: • Develop and execute recruiting channel strategy, in concert with Digital Recruiting Strategists • Effectively iterate and evolve channel strategy based on real-time insight, while engaging legal/medical/review boards in Pharma, Oncology and NIBR as appropriate. • Design, monitor and report on study-level KPIs and validate social media approaches for studies managed by NDR CoE. • Responsible for media strategies and all buying activities for digital recruitment • Stay ahead and on top of trends in social media platforms and innovations and educate key stakeholders across Novartis divisions Minimum requirements • 5 years experience in communications and/or social media, ideally in agency, consulting, or multinational corporate environment • >5 years, extensive experience in Digital & Social Media channel management and analytics, including direct experience with digital / social media media placement in Facebook, Google platforms, Advocacy groups, etc • Demonstrated track record of successful channel strategy implementation, evaluation and feedback loop to customers • Strong organizational skills with demonstrated ability to manage multiple priorities simultaneously • Proactive, entrepreneurial approach to recognizing needs and anticipating issues and solving problems WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitDATA & DIGITAL GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaCommunications & Public AffairsJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Postgraduate Scientific Communications

  • Novartis AG

  • 4051Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289620BRPosition TitlePostgraduate Scientific CommunicationsApply to Job Job Description 4! Four areas in global health and global drug development we are focusing on to make a difference in people’s lives. Your work will be important in helping more people understand our incredible commitment to bring transformative medicines to more people worldwide. Your responsibilities include but are not limited to: • Accountability for departmental internal and external communication deliverables as assigned, e.g. regular and ad hoc announcements, organization of internal and external events, departmental booklet. • Evaluation, optimization and implementation of departmental communication framework, aligned with the PHAD strategy. Drive pro-actively the implementation, pro-active own strong contribution with ideas for improvements. • Timely and constant strong communication and exchange with all associates within department and outside department as required. • Ensure correct, first-time-right and sound communication, e.g. ensure consistency and correct information in announcements, all details correct e.g. for data used in events. • Make pro-active proposals for events and tasks strongly fostering the team spirit. • Build a close business relationship and constructive partnership with colleagues through frequent and timely communication. Minimum requirements What you’ll bring to the role: • University Master degree in communications, journalism or science related fields • Excellent written and oral communication skills. Proficient in English, Fluent in language of country (e.g German and/or French) • Ability to work in a matrix organization interacting at different levels with the local and international organization • Act as an ambassador for Novartis mindset. Show and encourage collaborative, curious & courageous working style Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Head of Communications & Patient Advocacy - Oncology EGM

  • Novartis AG

  • 4051Basel

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288541BRPosition TitleHead of Communications & Patient Advocacy - Oncology EGMApply to Job Job Description As a key member of Oncology Emerging Growth Markets Leadership Team, NOCA LT, and the Patient Advocacy Leadership Network, this position will formulate and drive EGM Communications and Patient Advocacy strategies sup-porting the Novartis Oncology vision and mission aligned to business and Novartis priorities. • Enhance and protect Novartis Oncology’s reputation with key external stakeholders, particularly Patient Advocacy Groups and social/traditional media. • Inspire and engage associates across EGM around the Novartis Oncology strategy, key product and pipeline milestones, patient oriented initiatives, and the culture movement. • Work across EGM to develop a more ‘patient focused’ value chain from to drug de-velopment to market access and reimbursement to improve patient outcomes and Novartis Oncology reputation. • Collaborate across the Novartis Comms & Advocacy enterprise, build a world class Communications and Patients Advocacy function in key countries across EGM by pulling through strategies, aligning to business priorities, and nurturing/developing top functional talent. Your responsibilities include, but are not limited to: • Provide Communications strategy and programs aligned with the EGM Disease Area strategy teams on priority launches, growth brands, adapt Global campaigns for EGM, develop and lead EGM campaigns. • In collaboration with the Public Affairs and Market Access teams, develop and implement communications strategy to support the EGM position on priority policy issues that help evolve health care and improve patient access and outcomes. • Proactively identify opportunities for EGM leaders to engage externally with stakeholders and to increase visibility in influential forums, e.g. news media, panels, committees • Represent Novartis in appropriate patient-focused forums and other bodies/stakeholder groups that are patient-focused or have patient-focused initiatives. • Collaborate with the Global team input to build strategy, messaging, content and tools/templates to aid leadership in addressing key challenges facing business unit from external stakeholders. • Actively manage issues in EGM by providing communications strategy, stakeholder engagement plans as needed as well as related messages/materials • Collaborate with Global OBU Comms team, and Group comms as appropriate, in devel-oping responses to top-tier media inquiries in close collaboration with Novartis Oncology senior leadership, oncology media relations lead and corporate media relations team. • Develop and implement an inspiring and engaging strategic internal communications plan for EGM focused on driving performance against Oncology objectives, enabling a patient-centric business and driving the Novartis culture movement. • Improve Perception of Novartis Oncology as leading innovator, strong partner and corporate citizen with key external stakeholders as appropriate/needed • Enhance and improve the reputation of Novartis Oncology as a leader in providing patient access to medications. • Represent Novartis Oncology EGM on strategic patient and professional boards to advance the reputation of Novartis Oncology as appropriate/needed • Drive and align EGM T and relevant cross functional teams (marketing, medical, market access and public affairs) to ensure agreed deliverables are achieved support the objec-tives of the Commitment to Patients and Caregivers • Establish and provide a strategic framework how to conduct Patient Relations activities and help drive activities within the framework across EGM and within countries. Minimum requirements What you’ll bring to the role: • University degree required, with Masters preferred or MBA English (fluent), at least one other language covered in the region is a merit • Minimum of 10-15 years experience in the pharmaceutical industry, including Oncology experience, and proven track record as senior communications and patient advocacy leadership. • Understanding of key trends in both internal and external environment with an impact on traditional and social media and patient advocacy engagement • Understanding of the needs and behaviors of a broad variety of stakeholder groups, including patients and their families/caregivers, consumers, medical pro-fessionals, tradit • Proven ability to build and maintain effective working relationships with key inter-nal stakeholders, including commercial, medical affairs and leadership • Strong orientation toward cross-functional alignment and collaboration • Demonstrated communication skills including ability to influence others, champion change and be a thought leader • Experience in large, complex markets • Fluency in English (additional languages preferred)DivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaCommunications & Public AffairsJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

14.02.2020

Novartis AG

Global Public Affairs Director for Biomedical Innovation

  • Novartis AG

  • 4040Basel

  • 14.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289437BRPosition TitleGlobal Public Affairs Director for Biomedical InnovationApply to Job Job Description 8! The number of launches planned over the next 2 years. Your business acumen and communications mastery will help the world understand what these medicines do, why they matter and how Novartis is striving to reimagine Medicine. This position will lead development of policy concepts and advocacy tools to shape business critical external polices and political environment in support of biomedical innovation. Partner with Novartis business and functional experts to enable ONE voice approach in global advocacy. Your responsibilities: - Partner with Novartis business units, Corporate strategy and Corporate communications to identify business critical external policy areas and political developments, including reputational opportunities and challenges. - Be a trusted partner for Novartis business to provide input on political environment and developments, which are relevant for R&D and business decisions - Lead enterprise-wide strategy for the development of policy concepts and advocacy tools to enable Novartis to deliver on its strategic objectives for Biomedical Innovation. - Collaborate with functional experts across divisions to ensure high quality, timely input to policy concept development. Facilitate allocation of topics to functional subject matter experts as needed - Shape external policies and political environment relevant for Biomedical Innovation, including novel treatment options and pipeline compounds. Support capability building within regions and countries to ensure global concepts are adequately translated into local context. - Lead alignment of global franchise PA, regional PA and functional experts to enable ONE voice approach in global advocacy. - Participate in high-level round-tables, panels, stakeholder engagements, etc to advocate for Novartis positions with key stakeholders - Provide high quality and timely input to above country policy setting/ influencing bodies such as OECD, WHO Drive Novartis priorities through trade associations (PhRMA, EFPIA, IFPMA) by staffing Novartis board members and participating in key strategic committees Minimum requirements What you’ll bring to the role: - Advanced university degree in natural sciences (PhD preferred) - At least 5 years industry experience in relevant function plus ideally 3 years experience in public affairs including advocacy. Preferably 8+ years in industry - Fluency in English and at least one other major European language - Ability to conceptualize complex scientific topics and translation into effective advocacy messages/ tools. - High degree of business acumen to identify business relevant external policy areas - Impact on relevant external policy decisions to enable Novartis to deliver on its strategic priorities Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitNOVARTIS CORPORATE AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaCommunications & Public AffairsJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

14.02.2020

Novartis AG

Senior Corporate Executive Talent Scout

  • Novartis AG

  • 4051Basel

  • 14.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID287904BRPosition TitleSenior Corporate Executive Talent ScoutApply to Job Job Description 105,000 people are reimagining medicine at Novartis, and you will play a key role in helping us to continue build great teams. We have an immediate need for a Senior Corporate Executive Talent Scout to work in a newly created global position. In this highly visible strategic and tactical position your focus will be on the development of strong external talent pipelines for succession plans to support top level leaders and their leadership teams. You will be working with senior leaders at Novartis across multiple divisions, playing a pivotal role establishing the foundation and framework of a proactive external talent pipelining and relationship management processes. Your responsibilities include, but are not limited to: • Drive the Talent Pipeline Relationship Management responsibility by engaging high-quality passive talents, assessing their interest and suitability for current or future key positions at Novartis. Subsequently refine talent pools and leverage continuous candidate engagement opportunities. Establish strong candidate relationships to focus on candidate long-term career objectives in addition to short term job opportunities. • Identify high potential candidates, by utilizing all available candidate sources globally. • Provide professional level talent mappings for internal business benchmarking that will be utilized as a starting point for external Talent Pipeline Relationship Management activities. • Leverage opportunities with candidates to prompt career conversations, facilitate information exchange and to address and identify candidate career aspirations. • Be an active part of the global team of Novartis Executive Talent Scouts, which will include working to support each other on various initiatives and campaigns across the globe. Minimum requirements What you’ll bring to the role: • A track record of excellence in talent scouting and relationship management • Good cultural awareness to interact with international candidates and internal colleagues • Expertise in sourcing and screening of commercial talents while displaying a pro-active, tenacious and innovative approach to finding the talent. Desirable requirements: • Talent acquisition and scouting experience within the pharmaceutical or biotech industry. • At least 7 years of experience as an external recruiter or internal talent acquisition professional. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNBSBusiness UnitHR NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaHuman ResourcesJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

14.02.2020

Novartis AG

Global Program Head, Ophthalmology

  • Novartis AG

  • 4051Basel

  • 14.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288890BRPosition TitleGlobal Program Head, OphthalmologyApply to Job Job Description 125 countries and ~200 million patients each year receive Novartis’ ophthalmology products. We focus on changing the practice of medicine, enabling those living with eye disease to see how wonderful the world is. We are the largest of Pharma's innovative medicines franchises in terms of sales and offer patients one of the broadest portfolios of medicines treating the front and back of the eye. Novartis Ophthalmology is the global leader in the specialty with leadership positions in Retina, Glaucoma, Infections/Inflammation, and Allergy. We are a trusted partner in eye care, building on the extensive portfolio and continually pioneering new solutions to transform the lives of patients. As our Global Program Head (GPH) you will have final accountability for the innovation, strategy, operations, and related development deliverables for a Global Program (more straightforward programs) or a component of a larger Program (e.g. Multi-indication - e.g. AIN, ACZ or multifaceted due to regional complexity - e.g. NVA/QVA), within a designated disease/clinical area. You may also be engaged as a limited part of their role (with close supervision of their manager) for support of pre-PoC programs. The predominant responsibility is to lead a multidisciplinary team of functional experts focused on securing global regulatory approval, market access and optimized commercial value of the program while ensuring this is achieved with a high quality, full compliance (internal and external, e.g. regulatory, requirements) within budget and in a competitive and timely manner, utilizing both the internal or other identified expert resources necessary for success. Beyond your in- project responsibilities, you will be required to provide a strong and consistent support to the goals of the Franchise Leadership Team and to participate in critical development-wide management initiatives designed to shape the structure and processes of the organization. Most GPHs would start at this level (especially from external sources or non- Development roles unless they have clear GPH experience at this level or above). Your responsibilities will include: • Establish short and long range project vision and strategy • Ensure alignment cross global functions, regions and CPOs in regards to strategy and direction • Leverage knowledge, experience, understanding of external stakeholders, internal team capabilities and portfolio needs to develop a compelling, innovative vision and strategy for the program • Establish program strategy and execute implementation through milestones and decision points by leveraging cross-functional teams • Anticipate internal and external drivers of changes to strategy, and respond by making well judged and rapid revisions to program/portfolio strategy • Interact with Franchise Leadership Team, IMB and other management boards (i.e CLT) to secure internal stakeholder buy in to vision and strategy under supervision of a Sr. GPH • Develop and maintain a key communication strategy for investor relations and external communications around the program in cooperation with the Development and Business Franchise Heads • Actively coach and partner with direct reports to build and implement individual development plans and conduct their performance appraisal discussions in close partnership with the line-function heads [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Doctoral degree or equivalent, MD preferred • Minimum of 5 years of drug development experience, including experience in Global Program Teams and with dossier submission for new or supplemental indication • Leadership of multidisciplinary Teams, Clinical Background relevant to the Programs in the Development Franchise (Medical Training or Experience on Program Teams), Experience in product registration and major Health Authority interactions WHY CONSIDER NOVARTIS? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis!DivisionGlobal Drug DevelopmentBusiness UnitOPHTHALMOLOGY DU GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

14.02.2020

Novartis AG

Administrative Expert

  • Novartis AG

  • 4051Basel

  • 14.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID287929BRPosition TitleAdministrative ExpertApply to Job Job Description 50 Million! That is the number of how many secondary prevention patients worldwide do not achieve LDL-C lowering goals and remain at increased cardiovascular risk despite being on current standard of care. This position will be responsible for managing – i.e. planning, coordinating and communicating – complex administrative and organizational assignments; as well as dealing with company relevant very confidential material, data and information. Your responsibilities: • Deals with complex administrative and organizational assignments independently and takes care of general administrative tasks. • Screens, deals with and replies to correspondence, triages email, reminds and follows up topics as necessary to be taken care of by the manager. Is responsible for proper filing. Takes care of address databases, data synchronization. Picks up and deals with manager’s phone messages. • Takes proactively care of manager’s schedule. Prioritize people and meetings, proactively follows up with issues, timelines, etc.; schedules appointments on manager’s or own behalf according to strategic planning processes and overviews process related deadlines, organizes and supervises department specific processes. • Deals with meeting organization (logistics and agenda, records action items and assists in the development of documents and power point presentations) • Composes, types and edits a variety of correspondence, reports, memoranda and other material for the brand directors and the brand team members • Deals with all issues regarding travel arrangements, itinerary, meetings, bookings of tickets, expense claims, etc. • Informs, advises and supports the team, colleagues and associates from outside the team on processes, guidelines and services that are specific to the franchise and brand teams and to Novartis in general. Accommodates customers’ specific needs. Is a professional partner to people within and outside the department, at the headquarter and globally. • Absolute confidentiality and discretion in relation to various issues as: recruiting, interviews, organizational matters, company deals, contract negotiation, etc. is required. Minimum requirements What you’ll bring to the role: • Commercial training (e.g. Swiss Association of Commercial Employees, business school) or equivalent (e.g. other vocational qualification. Higher and additional education a plus • Fluent written and spoken English. Knowledge of other languages a plus • Must have very good administrative skills/experience. • Experience as Administrative Specialist or additional career training. Well-versed with the latest Novartis administrative processes and Tools Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaFacilities & AdministrationJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

14.02.2020

Novartis AG

Head of Third Party Risk Aggregation and Insight

  • Novartis AG

  • 4051Basel

  • 14.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289448BRPosition TitleHead of Third Party Risk Aggregation and InsightApply to Job Job Description 10 000! It is the number of Novartis third party engagements every year across the globe which need to be assessed from a risk management perspective. The Third Party Risk Management (TPRM) framework ensures that Novartis is conducting business with Third Parties who align to Novartis’ ethical standards and needs to manage reputational, regulatory and financial risks. A robust, proportionate and proactive process to qualify and manage third parties, by which Novartis protects their business and their patients, achieves this outcome. Improving the ability to aggregate risks will improve their resolvability. Reporting to the Head of Strategy, Human Rights and TPRM, the Head of Third Party Risk Aggregation and Insight is responsible for evolving the TPRM framework in order to maximize the value equation of our understanding of Third Party risks. This work drives the evolution towards ever more robust risk management environment assuring the Board of Directors, Leadership and Operations that systems are in place to effectively understand and manage risk exposures. Your responsibilities: • Develop strategies and implement initiatives to ensure that contemporary risk management approaches underpin and support the company’s ambition and culture; • Drive synergies to harmonize risk management outcomes, maximize the value of Novartis’ understanding of Third Party risk exposures at the identification and monitoring stages, and it’s impacts on society; • Instil quantitative approaches to TPRM’s framework, to standardize and aggregate risks for top management overview; • Lead and manage activities to achieve the above outcomes, including cross-functional stakeholder identification and management, work plans definition and final outcomes accountability; • Lead innovation in third party risk management, understanding trends from other companies, the evolution of regulation, and the opportunities arising from data and digital; • Reduce the probability and severity of losses resulting from third party risk management weaknesses; • Contribute to the improvement of the organisation’s overall quality of strategic planning through the enhanced ability to manage third party risks of new products and services; • Oversee that senior management third party risk reports meet the requirements and provide the right level and type of information to define and monitor adherence to risk appetite; • Ensure senior management is receiving the right balance of detail and quantitative versus qualitative information; • Support design of external reporting on third party risk management and impact on society; • Increase awareness of Third Party risk within key stakeholders. Minimum requirements What you’ll bring to the role: • Degree in banking, insurance, risk management, business, economics or related discipline required • Fluent English (oral and written) • Overall experience of 10+ years in risk management, including 2+ years’ experience managing innovative projects • Experience operating in complex matrix organisations • Capability to design/change risk management frameworks based on actual company needs • A strong track record in delivering innovating approaches • Capability to influence others and lead cross-functional teams without direct authority in matrix environments • Well-developed business partnering and stakeholder management skills • Capability to extract relevant insights and engage with top management. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitETHICS, RISK & COMPLIANCELocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

14.02.2020

Novartis AG

Senior Manager R and D Internal Audit

  • Novartis AG

  • 4051Basel

  • 14.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288094BRPosition TitleSenior Manager R and D Internal AuditApply to Job Job Description 125,000 unique individuals work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose: to Reimagine Medicine for millions of patients around the world. Come and join the team. Internal audit aspires to be a trusted assurance and advisory provider, and a talent pool driven by purpose to better support the business in serving our patients. The R&D Auditor Role within Internal Audit offers you an opportunity to develop leadership skills, business acumen, and risk awareness through hands-on audit engagements within NIBR and GDD. You will benefit from exposure to new areas around enterprise risk management, risk-based decision-making and evaluation of company controls. Furthermore, you will have opportunities to engage with senior leaders across the Novartis organization and develop skills around conducting risk assessments and leading advisory engagements to help the R&D organization meet its objectives. In addition, Internal Audit actively supports your development with training and coaching to enhance your auditing and leadership skills. • Lead effective audit teams throughout assignments in different divisions and functional areas taking responsibility for the team members, providing support and encouragement for good performance while maintaining an appropriate work-life-balance. • Understand key company policies that IA provides assurance on, including their implementing guidelines and procedures. • Apply effective project management skills to audit assignments in order to deliver work which meets quality standards, deadlines and the expectations of stakeholders. • Identify root causes of control issues. Investigate, analyse and test possible solutions or measures for improvement. • Prepare audit reports, review and agree issues with responsible management. • Establish and maintain key-contact relationships with the management in assigned countries and/or functional areas of responsibility to support the Regional Head Internal Audit (RHIA) in assessing risk across the region and developing the annual audit plan. • Lead the risk-prioritized planning of standard operational audits and support the Director of R&D Audit and the RHIA in the planning of complex audits on enterprise risks without pre-defined control frameworks. • Build effective business partnering and advisory relationships with senior management and with managers in the relevant functions, while maintaining the independence and objectivity of self, team and the IA function. Perform special projects and lead advisory initiatives to support the R&D organization. • Coach team members and guest auditors, and provide technical support and feedback. Minimum requirements • Professional degree (MD, PharmD, PhD) or equivalent experience in research and development, and/or background in Finance/Accounting/Auditing with exposure to R&D Activities • Fluent in English: oral and writing; additional languages a plus • Professional degree (MD, PharmD, PhD) or equivalent experience in research and development • Significant leadership experience in managing teams and projects • At least 4-6 years business experience, particularly in research and development on local/regional/global initiatives or internal audit experience in These areas • Willingness to travel (~40%+) WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitBUSINESS ASSURANCE AND ADVISORYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaAudit & FinanceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

14.02.2020

Novartis AG

TM Attorney

  • Novartis AG

  • 4040Basel

  • 14.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288099BRPosition TitleTM AttorneyApply to Job Job Description 750 000 000 ! This is the number of patients that our products reach every year and patients are at the center of all we do. All products of Novartis bear our company name which stands for the company’s vision and inspiration: to reimagine medicine! As part of the Trademarks & Domain Names Team at corporate level, this role is critical in protecting and maintaining the reputation of our company. At the same time in the modern world, products, even pharmaceuticals, are present online and in this role you can directly contribute to online defense and enforcement. This role safeguards Novartis’ reputation and the safety of patients which could be affected if products are altered during their movement between different countries. Provide trademark, copyright and domain name legal services and counseling to all relevant stakeholders of the Corporate Trademark and Domain Names Team. • Manage all core aspects of the assigned global trademark, copyright and domain name portfolio(s) independently and perform more complex trademark and related activities with minimal supervision. • Act as trademark, copyright and domain name subject matter expert for the assigned port-folio(s) and counsel on all trademark, copyright and domain name matters as they affect the business; for example, clearance, protection, enforcement, licensing, acquisitions, divestments, regulatory, etc. • Ability to counsel on all related matters as they affect the business; integrate and apply significant trademark concepts and activities, e.g., spot issues independently; assess business and legal risks in complex trademark and copyright topics, including in digital medicine/healthcare projects; and handle licensing, due diligence and contract review in transactions without supervision • Manage trademark and domain name litigation according to the agreed process and assist with coordinating parallel import and anti-counterfeiting activities. Act as valued strategic partner to the business to ensure business goals are met in an efficient and timely manner • Contribute to the development of guidelines, policies and procedures in trademark, copy-right, domain name and related areas of practice and ensure implementation • Actively contribute to drive divisional and cross-divisional projects to enhance the global performance of the IP Department. • Effectively co-operate to build and strengthen partnerships with all areas of the business with which the function interacts in line with the agreed guidelines, policies and procedures Minimum requirements • Bachelor, LLM in Law or equivalent English, additional languages a plus • Experience in EU trademark law and enforcement is required and in US trademark law / enforcement is preferred • Experience in transactional matters, litigation and day-to-day counseling as it relates to trademark, copyright, domain name practice is required • Ability to counsel on all related matters as they affect the business; integrate and apply significant trademark concepts and activities, e.g., spot issues independently; assess business and legal risks in complex trademark issues; and handle licensing, due diligence and con-tract review in transactions without supervision • Ability to manage opposition proceedings independently, and manage standard trademark and domain name litigation according to agreed policies; independently identify relevant legal issues and apply legal principles; provide strategic direction based on cost/benefit/risk analyses; and negotiate and draft settlements WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitGROUP LEGALLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

Trademark Attorney I

  • Novartis AG

  • 4040Basel

  • 12.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID286308BRPosition TitleTrademark Attorney IApply to Job Job Description 750 000 000 ! This is the number of patients that our products reach every year and patients are at the center of all we do. All products of Novartis Pharma have names which are carefully selected and protected with the aim to avoid confusion and medication errors. As part of the Trademarks, Domain Names and Copyright Center of Excellence, this role is critical in creating, protecting and maintaining future brands of the company. At the same time in the modern world, products, even pharmaceuticals, are circulating a lot between countries. This role safeguards Novartis’ reputation and the safety of patients which could be affected if products are altered during their movement. • Contributes to the global performance of the Pharma IP trademark center of excellence • Manages all regular aspects of the assigned trademark portfolio(s) and the parallel trade notifications with supervision as needed, and represents the company before trademark authorities (where appropriate) • Assists more senior trademark practitioners with counseling for all trademark matters as they affect the business including in collaboration with other stakeholders such as regulatory and legal • Assists in management of trademark litigation, especially in parallel trade according to the agreed processes and contributes to the development of trademark policies and procedures and assists with implementation • Effectively cooperates with all associates within the Global Novartis trademark function in line with the agreed policies and procedures; builds partnerships. Minimum requirements Education: Law Degree or Business Law Degree. Bar admission in any country would be a plus. Experience: • At least 2-3 years’ experience as IP / trademark attorney / specialist in a cross-cultural, cross-functional global/regional environment ideally gained within a pharmaceutical / biotech / life sciences company and/or in a law firm representing healthcare & technology clients. • A prior experience in parallel trade matters would be appreciated Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGlobal LegalLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

Clinical Development Director, Hepatology

  • Novartis AG

  • 4051Basel

  • 12.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288894BRPosition TitleClinical Development Director, HepatologyApply to Job Job Description 1 specialty areas, hepatology! we aim to transform patient care with life-changing, innovative therapies that provide patients with a longer & healthier life. As our Clinical Development Director (CDD) you will be the clinical leader of defined program level activities (e.g. submission activities, briefing books etc.), and/ or indication related clinical trial(s), under the leadership of the (Sr.) GPCH. You may lead a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase). Your responsibilities will include: • Provide clinical leadership and strategic input for all clinical deliverables in the assigned project or section of a clinical program if applicable. Clinical deliverables may include clinical sections of individual protocols or sub studies consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications • Lead development of clinical sections of trial and program level regulatory documents (e.g., Investigator’s Brochures, briefing books, safety updates, submission dossiers, and responses to Health Authorities) • Drive execution of the section of the clinical program in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, if applicable • Oversee/conduct ongoing medical and scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from Medical Lead • May be the Program Manager of other associates (e.g., CSE) • Support (Sr.) GPCH in ensuring overall safety of the molecule for the assigned section, may be a core member of the Safety Management Team (SMT), and support overall program safety reporting (e.g., Periodic Safety Update Reports (PSURs), Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety • Support the Therapeutic Area Head (TAH) by providing medical input into IDP and CTP reviews and contributing/driving development of disease clinical standards for new disease areas. May take on other TA responsibilities as directed by the TAH • As a clinical expert, support the (Sr.) GPCH or TAH in interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, data monitoring boards, advisory boards, patient advocacy groups), internal stakeholders (e.g., CTT, Research, Translational Medicine, Global Medical Affairs, Marketing, HE&OR), and internal decision boards • May work with NIBR (Novartis Institute of Biomedical Research)/ Translational Medical Sciences) to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L (Business Development & Licensing) including target identification and due diligences together with other medical matters, as needed [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Advanced degree in life sciences/healthcare (or clinically relevant degree) is required • PharmD, or PhD strongly preferred • ≥ 7 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV. ≥ 3-5 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry • Advanced knowledge of assigned therapeutic area • Proven ability to establish strong scientific partnership with key stakeholders • Thorough knowledge of GCP, clinical trial design, statistical analysis methodology, and regulatory/clinical development process • People management experience preferred, this may include management in a matrix environment. Global people management experience desirable WHY CONSIDER NOVARTIS? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis!DivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

Cheminformatics Expert (80-100% )

  • Novartis AG

  • 4040Basel

  • 12.02.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID287801BRPosition TitleCheminformatics Expert (80-100%*)Apply to Job Job Description 6500! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. We are seeking a unique cheminformatics expert with the skills, experience and passion to transform the combination of chemical and biological information into new knowledge and disruptive insights. You will be a member of our global Computer-Aided Drug Discovery (CADD) group, an interdisciplinary team of expert molecular modelers, cheminformaticians, and data scientists. In this role, you will work with and guide other domain experts to develop and improve novel as well as classical cheminformatics and data science approaches. You will also embedded into drug discovery teams to uncover insights to real-world drug discovery problems and innovate paths to new medicines. Responsibilities will include but are not limited to: • Develop tools and workflows for conducting comparative analysis among Novartis’ diverse data sources as well as generalizing and speeding up cheminformatics and CADD approaches developed in-house as well as externally. • Implement methods for extracting patterns and correlations from both internal and external data sources using cheminformatics toolkits • Enable open-source solutions (databases, toolkits and methods) for internal use and implement cutting-edge published scientific methods. • Interact with interdisciplinary project teams to drive effective decision-making by mining of predictive models • Work as part of a global group of cheminformatics experts and data scientists and guide local experts to execute on the global digital strategy • Keep ahead of scientific literature and interact with internal and external scientists to integrate novel data science technologies Minimum requirements What you'll bring to the role: • Advanced degree (M.Sc. or higher) in cheminformatics, computer sciences, mathematics, computational chemistry, computational biology, bioinformatics, data science and machine learning, statistics • Fluent in English • Proven track-record to work with and develop modern and classical cheminformatics methods and in depth experience with open-source cheminformatics toolkits such as RDKit • Strong programming experience (preferred Python, R, C++) preferably in Linux and high-performance computing environments • Hands on experience with web services, database integration and the integration of open-source code to produce solutions in a global enterprise environment ranging from fast prototyping to production quality level • Provided leadership for ad-hoc data analysis, visualization and statistical support in different areas of the drug discovery process and experience to closely interact with and understand scientific software engineers and other experts in the fields of computer science Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNIBRBusiness UnitGlobal Discovery ChemistryLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

Tierpfleger (80-100%)

  • Novartis AG

  • 4040Basel

  • 12.02.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID287581BRPosition TitleTierpfleger (80-100%)Apply to Job Job Description Bei Novartis arbeiten 105'000 Personen mit unterschiedlichen Bedürfnissen und Ambitionen, die auf ein einziges inspirierendes Ziel ausgerichtet sind: Reimagine Medicine für Millionen von Patienten auf der ganzen Welt. Derzeit suchen wir eine(n) Tierpfleger(in) - werden Sie jetzt Teil unseres Teams! Zu Ihren Hauptaufgaben gehören: • Ist Ansprechpartner / Auskunftsperson für das Laborpersonal (z.B. über die Unterbringung der Nager, Nutzung von Käfigwechselstationen etc.) • Arbeitet selbstständig nach Tierschutzgesetzgebung (Gesetz, Verordnung). Arbeitet selbstständig nach Novartis SciOps/LAS Qualitätsrichtlinien (z.B. HSE, SOPs), Hygienevorschriften (Hygiene-Konzept) und instruierten Anweisungen der Vorgesetzten und Forschergruppen. • Stellt Versuchstiere gemäss Anweisung des Laborpersonals für das bevorstehende Experiment entsprechend dem Wunsch nach Ort und Zeit bereit. Transferiert ankommende Tiere in den Tierraum, packt sie aus gemäss Anweisung (Tierschutzgesetz, maximale Anzahl Tiere pro Käfig) und setzt sie in geeignete Haltungskäfige um. • Tägliche Tier- und Käfigkontrolle, Protokollierung von Raumtemperaturen, Luftfeuchtigkeit, allg. Reinigungsarbeiten, besondere Vorkommnisse, etc. Macht per Telefon und /oder E-Mail oder entsprechendem Tool Meldung von kranken oder verletzten Nagern an den Veterinärdienst. Euthanasiert Versuchstiere auf Anweisung von Vorgesetzten oder Forschern • Tätigt internen Tier- und Materialtransport mit firmeneigenem Fahrzeug (Kat. B). Bereitschaft für Sa/So- und Feiertagsdienst (365 Tag-Betrieb). Nimmt an den Weiterbildungsveranstaltungen LAS teil und/oder bildet sich laufend am Arbeitsplatz im Rahmen des Aufgabenspektrums weiter. Minimum requirements Was ist notwendig für diese Funktion: • Ein- oder mehrjährige Tierpflegerausbildung oder gleichwertiges Training • Fahrzeugführerausweis Kat. B von Vorteil • Deutsch Grundkenntnisse vorausgesetzt • Englisch Grundkenntnisse vorausgesetzt • Erfahrung im Umgang mit Kleintieren (verschiedener Spezies, mehrere Teilgebiete der Zucht und Haltung von Versuchstieren). Warum Novartis? 750 Millionen - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. Wir sind Novartis. Kommen Sie zu uns und denken Sie Medizin mit uns neu.DivisionNIBRBusiness UnitCFOLocationSchweizSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaForschung & EntwicklungJob TypeVollzeitEmployment TypeUnbefristet Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

Internship ESO BT&A

  • Novartis AG

  • 4040Basel

  • 12.02.2020

  • Praktikumsstelle

Back to Previous Page Job ID289236BRPosition TitleInternship ESO BT&AApply to Job Job Description 365 days a year, our global manufacturing and supply network works to ensure we continue to deliver key medicines that enable our patients to live longer, healthier lives. Your responsibilities will include: • Support the global External Supply Operations (ESO) Biotechnology and Aseptics Operations Team • Perform Productivity Analysis • Co-ordinate Operational Improvement Project activities • Prepare reports and presentations on improvement opportunities to allow appropriate leadership decision making and drive change Duration: 9 months Minimum requirements What you will bring to the role: • University studies in the field of biotechnology, pharmaceutical engineering, or pharmacy • Preferably close to graduation at Bachelor or Master level • Fluent in English required • a plus basic Operational Excellence knowledge • advanced skills in MS office • good communication and facilitation skills Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNovartis Technical OperationsBusiness UnitNTO EXTERNAL SUPPLYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

Investor Relations ESG Director (40-60%)

  • Novartis AG

  • 4040Basel

  • 12.02.2020

  • Teilzeitstelle 40-60%

Back to Previous Page Job ID289041BRPosition TitleInvestor Relations ESG Director (40-60%)Apply to Job Job Description More than $50bn of net sales, more than $12bn of net income, 155 countries where our products are sold. Join Novartis Investor Relations team and become a relationship builder, an adviser to senior management, creative with communicating strategic, operational and financial information whilst exercising judgement and pragmatism to deliver meaningful messages to all our stakeholders. This position will lead the implementation of the Investor Relations dialogue with the Environmental, Social and Governance (ESG) analysts to support a fair reflection and ESG evaluation of Novartis. The purpose is also to lead Investor Relations programs for senior management (including ECN) at bank conferences and roadshows. Monitor external trends by providing meaningful regular analysis and critical evaluations to be used by management. Support, educate and train senior management on latest events, trends so they are well prepared for all elements of communication with ESG investor and analyst community. Provide support with ESG relevant information for senior management and Board. Your responsibilities: • Strengthen relationships with our current ESG stakeholders through creation and execution of ac-count plans • Address inquiries from investors and analysts on ESG subjects in a timely manner, providing accu-rate and balanced information • Plan and support execution of management roadshows, bank conference participation, one-to-one meetings for ESG investor Events • Actively support Head of IR on ESG specific projects (e.g. on presentations, analytics) • Participate in ESG IR roadshows • Capture ESG investor/analyst feedback and share with IR team and appropriate management. • Train and prepare management for ESG Events Minimum requirements What you’ll bring to the role: - Ideally medical or science basic degree, and ESG / CR or equivalent postgraduate - English mandatory - 5+ years’ experience in ESG related topics, and Finance in the healthcare industry; investment banking, research analyst or asset management with healthcare background. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are open to receive applications from candidates willing to work on a part time basis of 40% - 60%. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitGlobal Corp. FinanceLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaAudit & FinanceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

Lab Head, Immunology of regulatory T cells (80-100 )

  • Novartis AG

  • 4040Basel

  • 12.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID286487BRPosition TitleLab Head, Immunology of regulatory T cells (80-100*)Apply to Job Job Description 1 out of 10 people are diagnosed with an autoimmune or autoinflammatory disease. This is why the Autoimmunity, Transplantation & Inflammation (ATI) Disease Area group at the Novartis Institutes for Biomedical Research (NIBR) is investing in the discovery of innovative and transformative therapies to improve the life of affected patients. As part of this effort, ATI is seeking an innovative and highly motivated senior scientist to initiate and guide research projects in the area of immune tolerance. Your Responsibilities: You will be responsible for leading a state-of-the-art laboratory of BSc/MSc level scientists to discover and develop novel therapies for re-establishment of self-tolerance in various autoimmune diseases. This will include the evaluation of ex vivo and in vivo approaches aiming at the induction of regulatory T cells. Your tasks will include: • Contribute to and/or lead early drug discovery projects within multidisciplinary teams up to clinical proof-of-concept studies in patients • Define and execute on innovative scientific strategies, test novel hypotheses and develop transformative therapies • Closely collaborate with scientists, clinicians, and technology experts across different departments in the global organization. • Your scientific work will continue to result in impactfull publications in peer-reviewed journals. Minimum requirements What you’ll bring to the role: • A PhD degree with several years of postdoctoral experience of research in immunology and autoimmunity • Significant scientific accomplishments and successful collaborations documented by publications in high-impact journals • Strong technical and theoretical background/expertise in human and mouse immunology • Proven track record of leadership, strategic thinking, creativity, and risk taking • Excellent communication, presentation and analytical skills Desirable requirements: • Experience as an independent research scientist in an academic setting and/or in the pharmaceutical/biotech sector • Proven success in independently initiating and leading projects in autoimmunity and inflammation, especially related to the biology of regulatory T cells and cellular immunology Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNIBRBusiness UnitAUTO/TRANS/INFL - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

Business Partner MENA / MEA region, Finance, Commercial, Export

  • Novartis AG

  • 4051Basel

  • 12.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288682BRPosition TitleBusiness Partner MENA / MEA region, Finance, Commercial, ExportApply to Job Job Description Responsibilities: • Define business partnering strategy for the specific Clusters/Countries and translate it into initiatives, activities, processes and guidelines • Work at regional and country level to drive respective initiatives and to anticipate future needs and opportunities • Establish positive relationship with the Clusters/Countries Leadership Teams to understand their needs and challenges, and to manage implementation of operational objectives and drive continuous improvement and innovation • Provide advice, recommendations, coaching and on-boarding to Clients’ Leaders/Managers, understanding needs and challenges and helping to achieve business objectives (e.g.: to General Managers, Heads of Finance and Supply Chain, Heads of Legal, Compliance Officers) • Define the essential product portfolio for the High Risk Markets • Lead the preparation and presentation of business cases related to Business Model changes to be approved by Division Pharma & ECN • Lead timely establishment of contracts for all commercial transactions with third parties • Lead the cross-functional Basel review and approval of Clients’ business decisions to fulfill customer demand, while working closely with partners at Country/sub-Cluster/Cluster/ Region/Global level • Implement High Risk Country supply model in alignment with Regions and MENA Task-force. Work with medical and regulatory affairs for sustainable patient access to essential medicines • Drive cross-functional collaboration between Legal, Finance, Credit Management, Supply Chain, Funds Flow, Tax, QA, DRA, Medical, DS&E, Patient Access, Public Affairs, HR and IT • Lead Basel Sales & Operations Planning process with Supply Chain, Finance and Clients • Drive the process to approve new distributors & support Clients for distributor coordination • Contribute to decide new local NPhS warehouses • Cultivate clarity of roles and responsibilities for decisions and activities which occur between NPhS Basel and its Clients and ensure timely Minimum requirements University degree, MBA or other first class education (e.g.: Business, Economics, Finance, Marketing) Fluent in English (spoken and written) Fluency/knowledge of other languages is an asset 10 years of managerial international experience, in multi-national companies, in Business & Finance areas, at Country/Region/Global levels WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma Services AGFunctional AreaAudit & FinanceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

Senior Legal Counsel IP Litigation

  • Novartis AG

  • 4040Basel

  • 12.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289318BRPosition TitleSenior Legal Counsel IP LitigationApply to Job Job Description 400 plus active IP litigations, and at least 50 new ones yearly, across a diversified and exciting portfolio of innovative and generic medicines, Novartis Group stands at the front of worldwide, sophisticated IP litigation critical for funding our mission-forward research and development while also providing unparalleled access to patients. Manage reporting for Novartis Global patent and other IP litigation by establishing and maintaining worldwide best-in-class processes and policies, including communication and legal requirements for SOX and other public reporting accountabilities; managing and providing thought leadership on key patent litigation and other IP issues; identifying and responding to patent and other IP legislative, litigation, and policy trends. IP Leadership / Management (50%): Participate in cross-functional team of litigators in development of strategies for key patent and other IP litigations; provide coaching & strategy review of patent and other IP litigations with Divisional IP litigation teams; work with Global Head IP, Global Head IP Litigation, Global Head IP Policy, and Global Head IP Strategy on special projects, including preparation of papers, positions, and comments to new patent policy and other IP initiatives; hold and participate in internal and external meetings with IP-policy stakeholders; preparing patent and IP-policy papers, positions, and comments to new legislative initiatives; monitor and anticipate shifting legal and political developments and trends; engage in and coordinate defined lobbying activities worldwide. Reporting Management (30%): Manage internal SOX and other reporting practices for appropriate and complete disclosure of patent litigation and other IP matters important or material to Novartis Group; lead and manage development and authorship of IP sections to corporate quarterly and annual reporting; work with key internal stakeholders critical to reporting, including Group Legal, US Legal, and Finance; interface with outside counsel for opinions on disclosure and to ensure best practices; maintain a Group-wide overview on patent, other IP, and general litigation activities; coordinate information needs with Divisions, Communications, Global Public Affairs, and Investor Relations. IP Leadership / Management (20%): Manage and participate in Group Litigation Review processes, including review and comment on divisional patent and trademark litigation proposals and related external opinions, in particular for cross-divisional alignment and policy perceptions; contribute to Litigation and IP Policy practice teams, and lead select initiatives and projects within same; participate in Group IP and Global Litigation meetings; advocate internally and externally for NVS positions; support other Group and Divisional IP functions as needed and directed. Minimum requirements Law school graduate and qualified attorney-at-law (Bar member) in common law jurisdiction, legal doctorate preferred (J.D. or equivalent). Patent attorney qualification preferred, but not required. Fluency in English, some skill or proficiency in German a plus At least 7-10 years post-Bar experience required, including exposure to and participation in patent and other IP litigation proceedings in European countries and/or the United States. At least some experience managing reporting or consolidation of worldwide IP proceedings. Demonstrated writing abilities, preferably with oral advocacy experience. Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.DivisionCORPORATEBusiness UnitGROUP LEGALLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Lab Head - Molecular Imaging & Radio Ligand Therapy (80-100% )

  • Novartis AG

  • 4040Basel

  • 10.02.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID287633BRPosition TitleLab Head - Molecular Imaging & Radio Ligand Therapy (80-100%*)Apply to Job Job Description 6500! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Applications are invited for a Laboratory Head position in Oncology Research that will carry out cutting-edge research in the areas of molecular imaging and radioisotope-based therapies together with leading basic research groups within NIBR. The candidate will be responsible for small animal molecular imaging (PET/SPECT/uCT) and drug discovery pharmacology activities within the Radio Ligand Therapy portfolio. We seek an experienced, motivated and ambitious scientist wishing to continue a successful scientific career in a fast-paced drug discovery environment. The position is based at the Novartis Institutes of BioMedical Research (www.nibr.com) in Basel, Switzerland. The ideal candidate should have a strong background in the molecular imaging modalities: PET, SPECT and uCT and a solid expertise and knowledge in developing Radio Ligand Therapies with a proven ability to conduct multidisciplinary research in a competitive field and an excellent record of achievements. The successful candidate will have solid expertise with rodent in vivo models and is expected to play a key role in the establishment of novel rodent models for Radio Ligand Therapies in the field of cancer. Required skills and accountabilities: • Lead a laboratory with expertise in nuclear medicine and innovative imaging modalities including PET/SPECT/uCT • Perform biodistribution studies and metabolites analysis ex vivo • Engage in independent research that will lead to innovative findings and novel fundamental insights • Lead and manage cross-functional projects and external collaborations. Drive the project decision-making process, conceptualize and drive research projects to completion Minimum requirements What you’ll bring to the role: • Ph.D. in medical physics, bioengineering, biotechnology, pharmacology or related field • At least 5 years of experience in a drug discovery setting • The position requires excellent communication skills in English and the motivation to work independently within a global team Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNIBRBusiness UnitOncology NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Patent Attorney - Biology, Research & Development (80-100% )

  • Novartis AG

  • 4040Basel

  • 10.02.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID280136BRPosition TitlePatent Attorney - Biology, Research & Development (80-100%*)Apply to Job Job Description 30000+ active patent records! And 150+ patent applications filed annually! Are you curious and inspired to reimagine medicine as part of a collaborative and creative team of patent attorneys? Join our global R&D Intellectual Property team spread across 5 sites in the U.S. and Switzerland to make an impact on how we protect innovative medicines for patients WHAT YOU’LL BRING TO THE ROLE: • Provide clear, informed and sophisticated counseling to Novartis R&D clients (e.g., including Novartis Institutes for BioMedical Research (NIBR) and Global Drug Development (GDD) clients) on all IP matters, including opportunities to protect their inventions and to mitigate third party risks • Build and handle patent portfolios for Novartis R&D projects by identifying inventions and preparing, prosecuting, maintaining and defending patent filings for all inventions arising from R&D projects relating to platform technologies, biological targets, new biologic entities, manufacturing processes, and clinical development (e.g., formulations, additional indications, combinations) • Render legal opinions with respect to patentability, validity, and freedom to operate, and formulate patent strategies for Novartis R&D clients that secure IP protection, Freedom-to-Operate (FTO), and enable IP defense(s) • Apply deep expertise in national patent law and practice, including patent trends and case law developments, to devise patent strategies and advice • Understand other forms of protection relating to exclusivity, and applies as required • Build and manage external relationships with outside counsel and collaborators, including substantial interactions within a multicultural global patent function • Provide IP support for transactional projects, such as research collaborations and in-licensing opportunities, including advice on contract drafting and negotiation • Conduct due diligence assessments and counsel based on these assessments, including freedom-to-operate (FTO), infringement and validity analyses, and risk evaluation and mitigation • Direct the R&D Patents Search & Analytics team to provide integrated search support for IP and transactional activities • Effectively communicate with colleagues and leadership in the legal and IP function as well as the R&D organization • Conduct timely review of assigned external publication requests • Continue professional development and contribute to development of IP colleagues *Some restrictions on flexible working options may apply and will be discussed during interview if applicable Minimum requirements EDUCATION Minimum education: B.A., B.Sc. (or equivalent) in Biomedical Sciences or equivalent; Registered European Patent Attorney, preferably also EU-national Patent Attorney Qualification. Desirable education: M.S., Ph.D. or equivalent in Biomedical Sciences EXPERIENCE: At least 3 year experience as a Qualified European Patent Attorney in a law firm or in the research and development industry with significant responsibility for patent prosecution and counselling, including patent drafting and prosecution in the biotechnology industry. KEY CAPABILITIES • Strong scientific background in biological sciences; preferably including direct lab experience • Expertise in local (US or EP) and PCT law, filing process and prosecution practice; detailed understanding of counterpart EP or US law and other major global patent systems • Strong customer-service focus to build and sustain effective partnerships with key stakeholders and project teams • Effective analytical, presentation and communication skills • Proven ability to work independently as well as collaboratively in a team • Well-developed research and critical thinking skills, and sound decision-making abilities, with attention to detail to produce consistently accurate work • Strong organization and time management skills with flexibility, creativity, resourcefulness to successfully prioritize and manage multiple, competing priorities simultaneously • Interpersonal skills (partnership, influence/persuasion, teamwork) • Ability to incorporate global outlook and management of product life-cycle into decision-making process WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Global Medical/ Scientific Director - Lung

  • Novartis AG

  • 4040Basel

  • 10.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288300BRPosition TitleGlobal Medical/ Scientific Director - LungApply to Job Job Description 1 in 5 men and 1 in 6 women worldwide develop cancer during their lifetime according to the World Health Organization. In Oncology Medical Affairs we are working tirelessly to bring innovative cancer treatments to patients with our presence in four oncology treatment platforms. As Global Medical/ Scientific Director you will be the Medical Affairs leader for an assigned disease area, compound(s) and/or project(s) under the leadership of the specified disease area Global Group Medical Director. You will provide strategic direction to the region and country medical teams and ensure execution of the medical strategy and tactical plan in regards to a specific compound or project. The role requires broad scientific and therapeutic area expertise and business understanding to identify and address the needs of patients, HCPs and other stakeholders. Your responsibilities will include: • Participate in Integrated Disease Medical Team (IDMT) to gain strategic and planning alignment across regions and functions. You may be a core member of the Global Program Team (GPT) • Contribute to the establishment and implementation of policies and standards for global and local clinical studies as well as other activities defined in the Medical Plan for the therapeutic area (e.g. publication, registries, Medical Expert management) • Encourage and cultivate collaboration, and the optimization of resources across disease area medical teams • Manage all operational aspects and drive execution of Global Medical Affairs (GMA) clinical trials in partnership with global line functions, assigned clinical operations team members, and regional/country medical associates • For assigned compound/indications, work collaboratively across functions, within GPT to execute an integrated Medical Affairs plan including clinical trials, publication, medical education and medical information • Provide medical review and approval of key scientific communications, medical information documents and commercial documents within P3 legal and compliance regulations • Provide medical input on overall publication strategy and be a key member of the publication planning team providing GMA medical input on individual publication plans [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • MD required for Global Medical Director role; Global Scientific Director requires advanced life sciences degree (PharmD, PhD, etc.) • More than 3 years advanced knowledge in medical/ scientific area (Oncology, Hematology, Endocrinology preferred) • 10 years professional experience within the pharmaceutical industry, preferably in development and/or medical affairs function at a regional or global level • Developed and implemented global/local Phase II, III or IV trials • Experience of working in a matrixed, cross-functional, environment an advantage • Experience of Medical Experts relationship management is valued WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Global Professional Relations, Cardio-Renal-Metabolic

  • Novartis AG

  • 4040Basel

  • 10.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288570BRPosition TitleGlobal Professional Relations, Cardio-Renal-MetabolicApply to Job Job Description 50 Million! That is the number of how many secondary prevention patients worldwide do not achieve LDL-C lowering goals and remain at increased cardiovascular risk despite being on current standard of care. As part of Novartis, you are committed to reimagine medicine and be part of a remarkable team that shares the vision to transform clinical practice for patients with cardiovascular disease. You will also realize your potential while interacting with an outstanding employee community, working side by side with talented individuals and collaborating with the most respected academic institutions. Some of the best leaders in the industry will inspire you. This is a role waiting for you to put your own stamp on it. Your responsibilities will include: • Contribute to the identification and mapping of global key opinion leaders in collaboration with medical affairs, regions and key countries • Co-develop a strategic long term relationships and partnerships with leaders, key scientific societies and advocacy groups in collaboration with medical affairs, public affairs, regions and key countries • Supports the organization of major international congresses in collaboration with medical affairs, coordinates internal stakeholders [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Medical Doctor, or PhD • Strong interpersonal skills • Experience working with Cardiologists and scientific societies (US and Europe) • 8-10 years of Marketing and/or Medical Affairs experience with focus KOL/Stakeholder management/Congress Management WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Global Marketing Director, Cardio-Renal-Metabolic

  • Novartis AG

  • 4040Basel

  • 10.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288573BRPosition TitleGlobal Marketing Director, Cardio-Renal-MetabolicApply to Job Job Description 50 Million! That is the number of how many secondary prevention patients worldwide do not achieve LDL-C lowering goals and remain at increased cardiovascular risk despite being on current standard of care. As part of Novartis you are committed to reimagining medicines for patients with dyslipidemia and to helping realizing your potential and being part of a remarkable employee community. You will work with hardworking individuals - experts in their field and be inspired by some of the best leaders in the industry. This is a role waiting for you to put your own stamp on it. Your responsibilities will include: • Develop the launch strategy with the global crossfunctional teams, regions and key countries • Develop the vision, the aspiration and the positioning of the brand • Lead the development of the brand messaging and communication • In partnership with medical, build a robust scientific platform and engage with key experts in the field • In partnership with patient access, develop pricing options and innovative access models • Provides commercial input to product development, including new indications and life cycle management • Design and implement differentiate launch tactics • Collaborate with countries to ensure wide implementation [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you will bring to the role: • University degree in Science and/or degree in Business Marketing, master preferred • At least 10 years of sales and marketing experience, ideally a mix of both in-market and global experience • Launch experience – cardio and multi-country preferred • A passion for trying new approaches Desirable requirements: • An experience in the vaccines business would be a plus WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Investor Relations ESG Director

  • Novartis AG

  • 4040Basel

  • 10.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288476BRPosition TitleInvestor Relations ESG DirectorApply to Job Job Description More than $50bn of net sales, more than $12bn of net income, 155 countries where our products are sold. Join Novartis Investor Relations team and become a relationship builder, an adviser to senior management, creative with communicating strategic, operational and financial information whilst exercising judgement and pragmatism to deliver meaningful messages to all our stakeholders. This position will lead the implementation of the Investor Relations dialogue with the Environmental, Social and Governance (ESG) analysts to support a fair reflection and ESG evaluation of Novartis. The purpose is also to lead Investor Relations programs for senior management (including ECN) at bank conferences and roadshows. Monitor external trends by providing meaningful regular analysis and critical evaluations to be used by management. Support, educate and train senior management on latest events, trends so they are well prepared for all elements of communication with ESG investor and analyst community. Provide support with ESG relevant information for senior management and Board. Your responsibilities: • Strengthen relationships with our current ESG stakeholders through creation and execution of ac-count plans • Address inquiries from investors and analysts on ESG subjects in a timely manner, providing accu-rate and balanced information • Plan and support execution of management roadshows, bank conference participation, one-to-one meetings for ESG investor Events • Actively support Head of IR on ESG specific projects (e.g. on presentations, analytics) • Participate in ESG IR roadshows • Capture ESG investor/analyst feedback and share with IR team and appropriate management. • Train and prepare management for ESG Events Minimum requirements What you’ll bring to the role: - Ideally medical or science basic degree, and ESG / CR or equivalent postgraduate - English mandatory - 5+ years’ experience in ESG related topics, and Finance in the healthcare industry; investment banking, research analyst or asset management with healthcare background. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitGlobal Corp. FinanceLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaAudit & FinanceJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Research Scientist, Lab Animal Services (80-100 )

  • Novartis AG

  • 4051Basel

  • 10.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID287468BRPosition TitleResearch Scientist, Lab Animal Services (80-100*)Apply to Job Job Description 602! That’s how many research studies were performed by our small but driven team in 2019. This role is very technical and involves providing high quality in vivo scientific/technical support as well as training for a large number of projects in multiple disciplines. It is an excellent opportunity to collaborate across a wide range of disease areas within the Novartis Institutes for BioMedical Research (NIBR). Your responsibilities: • Ensure state-of-the-art animal experimentation with the highest ethical and technical standards: animal handling, substance application, clinical signs monitoring/scoring, organ sampling or implementation of novel technologies • Provide with interpretation of results, evaluation of data and design of the next experiment with limited input from supervisor • Closely and independently interact with scientists within NIBR providing efficient support and generating high quality in vivo data • Generate, review and understand experimental protocols, based on professional experience or continuous literature review • Responsible for pursuing continuous learning/professional development opportunities, improving/expanding skill set, and reviewing SOPs/techniques; Weekend duties, early morning or late evening dosing Minimum requirements What you’ll bring to the role: • You hold a life science bachelor or master degree (or equivalent) • You possess a good technical expertise working with small animals (>3 years) • You are an excellent teammate with a high level of flexibility • You strive for excellency and are proactive at identifying and implementing innovative ways • English required, German and/or French advantageous Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNIBRBusiness UnitCFOLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Scientific Associate - Pre-clinical molecular imaging (80-100% )

  • Novartis AG

  • 4051Basel

  • 10.02.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID287628BRPosition TitleScientific Associate - Pre-clinical molecular imaging (80-100%*)Apply to Job Job Description 6500! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Applications are invited for an associate position in an Oncology Research laboratory that will carry out cutting-edge research in the areas of molecular imaging and radioisotope-based therapies together with leading basic research groups within NIBR. The candidate will be performing small animal molecular imaging (PET/SPECT/µCT) and drug discovery pharmacology activities. We seek an experienced, motivated and ambitious associate wishing to continue a successful scientific career in a fast-paced drug discovery environment. The position is based at the Novartis Institutes of BioMedical Research (www.nibr.com) in Basel, Switzerland. The ideal candidate should have a strong hands-on background in the molecular imaging modalities: PET, SPECT and uCT and expertise in molecular medicine. The successful candidate will perform independent experimentation and data analysis and have solid expertise with rodent in vivo models and is expected to play a key role in the establishment of novel rodent models for Radio Ligand Therapies in the field of cancer. Responsibilities to include but are not limited to: • Perform pre-clinical innovative imaging studies including PET/SPECT/uCT • Complete in vitro characterization (e.g. plasma stability, protein binding, cellular uptake) • Perform biodistribution studies and metabolites analysis Minimum requirements What you’ll bring to the role: • Master degree in medical physics, bioengineering, biotechnology, pharmacology or related field • At least 5 years of experience with PET/SPECT/uCT imaging and in vivo pharmacology experimentation with mice and rats • The position requires excellent communication skills in English and the motivation to work independently within a global team Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNIBRBusiness UnitOncology NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Global Change Lead for NBS Transformation

  • Novartis AG

  • 4051Basel

  • 10.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288537BRPosition TitleGlobal Change Lead for NBS TransformationApply to Job Job Description 1 company – that is the journey Novartis is on in its quest to extend and improve people’s lives through reimagining medicine. We have a clear strategy: to be a focused medicines company powered by advanced therapy platforms and data science. We recognise our people drive our company and significant effort is being invested in unleashing their power through the transformation of our culture and our organisation. A number of significant changes are underway in our company with incredible energy from our top leaders. As our Change Management lead, you will be responsible for developing overall program level Change Management strategy for NBS (Novartis Business Services) Transformation. You will own and define the strategy with the NBS Transformation Lead to include the consistent methodology used, tools/tactics and governance of change management plans. Plans are designed to address key enablers and big tickets of NBS transformation that impact the successful mindset and behavior changes in support of achieving NBS aspiration to be the 4th generation business services organization. Further, you will work closely with the Change Management Leads at Bundle and country level to ensure the respective required change management plans are well defined and executed through across the organization, NBS and Novartis. Your responsibilities will include: • Ensure linkage to the NBS Aspiration in everything we do • Set standards for Change Management at all levels of the Program, building capability and coaching/ facilitating as required • Facilitate a Change Management Community of Practice • Fully aligned to- and supported by- Communications • Co-create and drive change plan and interventions at a program level • Manage cross-program risks regarding change • Act as trusted partner and thought leader to NBS transformation PMO on overall transformation strategy and execution • Develop and oversee strategic change management initiatives and plans, and drive implementation across all bundles and countries with consistency and strong collaboration • Educate and engage around the impact and benefits of transformation activities • Drive ownership and accountability amongst all managers and leaders to successfully drive Changes Core skills • Ability to create change management strategies and plans that engage associates on all levels, maximize employee adoption of the change and minimize resistance • Strong practical experience executing Change Management on large and complex global scope • Recognized as a leader within the community/change management space • Ability to develop strategic plans on managing change and coordinate with the PMO to execute against those plans • Knowledge of change management principles, methodologies and tools, including but not limited to good understanding of how people go through change and change processes, analytical skills and ability to oversee and interpret impact assessments, and ability to assess change readiness and identify/map key stakeholders • Know approaches and tools to handle resistance and elevate change/ engagement • Understanding for Change Management disciplines (e.g. People, Trainings, Developments, Communications, Engagement, Leadership and Org Design) and pulling the right capabilities and experts together to be impactful – both strategic and operational • Solid understanding of Novartis organizational processes, issues/challenges and processes (preferably) [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Minimum Bachelor degree, preferably Masters or equivalent qualifications • Excellent English spoken and written • 10-15 years professional experiences in the space of change management, organization development, supported by broader consulting, people and organization partnering and/or related areas • Strong experience with senior executive engagement and facilitation, strong influencing ability through consulting, communication and trusting relationship building skills • Proven analytical and conceptual skills, combined with ability to implement • Demonstrated expertise in OD (organisational development) and change management methodologies and (successful) global project delivery • Known for strong collaboration and networking with the broader People & Organization community and other stakeholders • External consulting and/or business leadership experience would be valuable WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionNBSBusiness UnitHR NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaHuman ResourcesJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

06.02.2020

Novartis AG

JUMP MBA Leadership Development Program

  • Novartis AG

  • 4040Basel

  • 06.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288569BRPosition TitleJUMP MBA Leadership Development ProgramApply to Job Job Description The newly created JUMP program (Join & Unleash My Potential) was created to offer future Novartis leaders a unique learning experience through a personalized professional develop-ment journey, with one of the world’s largest pharmaceutical companies impacting 799 million lives around the world. Spanning multiple countries over a 2+ years journey, each rotation will last 12 months giving associates the exposure to different Novartis businesses and functions. With each rotation and in line with background and interests of individuals, responsibilities will be increased and transversal projects will be assigned in order to accelerate knowledge growth of future Novartis leader. Jump Leadership Development Program Lead will be providing strategical support to the country Leadership team in Region Europe. It will lead the business development projects within a given scope of responsibilities (Market Access, Marketing, Business Franchise, etc). Jump Program Lead will be responsible for delivering transversal projects. The role will re-quire influencing stakeholders and bringing strategic thinking and creativity to drive innovation and challenge the status quo. The role will be open across Europe including Spain, UK, Italy, France, Germany, Switzerland and possible other European countries or clusters depending on challenges encountered. Jump Program Lead will provide lead and drive key projects, supporting multiple functions as well as ad-hoc requests which aim will be to improve daily business operations. Jump Program Lead will be exposed to multiple functions and leading cross-functional areas as: Finance, Health economics and Market Access, Digital, Medical, Clinical Trials, Marketing or Operations, depending on what business challenge which will be assigned to the project. The role requires close collaboration with all cluster functions, CPOs' leadership teams, Re-gion Europe teams & selected Global functions, proactive management of cluster governance ( LT VCs, meetings etc) and performance management processes (i.e. business reviews, strategic planning, budget). The role also provides leadership and project management expertise to ensure a successful execution of strategic initiatives. You will be responsible but not limited to: • Drive business operations activities (e.g., leadership meetings preparation), including agenda, time management, pre-reads, minutes, action plans and follow up. • Provide continuous support to Head of the selected country on an ad-hoc basis (e.g., business reviews, ECC preparation and any Global requests) in strong coordination with the other functions. Produce all briefings and ensuring that the Head of Country/Cluster is prepared at all times. • Coordinate / co-lead JUMP Project agenda in close coordination with CPOs, Region Eu-rope commercial team, Business Franchises and Finance. • Leading or cooperating on Country/Region Strategic Projects. Including project shaping (together with key functions involved), problem structuring, data gathering and problem solving, developing and communicating clear and actionable recommendations. • Coach the newly appointed Jumpers to facilitate their onboarding. • Taking care of proper internal communication and communication platforms (e.g. week-ly/monthly communication efforts, SharePoint site management, Town Halls, etc.) Minimum requirements • Master’s degree in Business Administration • MBA has to be completed by September 2020 • At least 5 years of relevant professional experience in a given field • Languages: fluent in English (written and spoken) is a pre-requisite, other European languages are an asset • Genuine interest in the pharmaceutical industry • Eager to discover different areas in Novartis and further develop within the company • Strong interpersonal, collaboration & communication skills • Team player and an agile learner • Happy to deal with ambiguity • Full mobility Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaBD&L & Strategic PlanningJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

06.02.2020

Novartis AG

Communications Manager

  • Novartis AG

  • 4040Basel

  • 06.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID287460BRPosition TitleCommunications ManagerApply to Job Job Description 100,000 unique individuals work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose: to Reimagine Medicine for millions of patients around the world. Your business acumen and communications mastery will help the world understand what these associates do, why it matters, and how Novartis is striving to reimagine medicine. The Purpose of this position is to achieve the most positive image for Novartis Pharma and its products with target audiences (key stakeholders, media, and professional organizations) through dissemination of Novartis key messages and communication plans. He/She has previous experience in these roles, together with a keen understanding of pharmaceutical communication needs. Key components for success are the ability to high level interaction with key stakeholders, provide product/communication advise, work closely and coordinate activities with commercial communicators; aligning strategy/ messaging as appropriate. You will be responsible but not limited to: - Work across priority areas as well as champion integrated thinking between comms, advocacy and social media. -Work together with brand teams to develop and implement strategic public relations/brand communications plans as an integral part of marketing planning and promo-tional mix. - Manage BU brands communications, including PR - Manage agencies and other PR / communication vendors. - Work together with other areas in the BU to manage and coordinate relationships with medical associations and patient advocacy to support strategic objectives in the BU. Minimum requirements What you’ll bring to the role: - University degree. Preference: Life science / Medicine - English – fluent, language of country – fluent - Extensive experience (>3 years) in communications / PR positions ideally in the healthcare sector including high-level involvement in media. Significant experience in communication positions and excellent abilities to understand Pharma communication concerns regarding public, media, patient relations. - Demonstrated skills to influence high level media and stakeholders. - Excellent written and oral communication skills. - Excellent persuasive ability to build strong stakeholder relationships for the company by optimally using available resources and personally influencing the environment. - Ability to work in a matrix organization interacting at different levels with the local and international organization. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionPHARMABusiness UnitGlobal CommunicationLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaCommunications & Public AffairsJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

05.02.2020

Novartis AG

Internship Pharmacometrics/Master or PhD

  • Novartis AG

  • 4040Basel

  • 05.02.2020

  • Praktikumsstelle

Back to Previous Page Job ID288292BRPosition TitleInternship Pharmacometrics/Master or PhDApply to Job Job Description 700! The number of days we can get therapies faster to patients applying Technology innovation. ggPMX is an open-source R package developed by the Pharmacometrics group at Novartis to produce diagnostic plots of nonlinear mixed-effect (NLME) models (https://github.com/ggPMXdevelopment/ggPMX). The package is available on CRAN and is currently compatible with Monolix and nlmixr software. Your responsibilities will include: In this project, you will work to extend the compatibility of ggPMX to NONMEM, based on existing specifications under the guidance of experienced quantitative scientists. NONMEM compatibility will enable to extend usage of ggPMX to three of the most popular NLME modeling software, an important and unique feature of our package. This will allow using ggPMX for all internal projects, facilitating productivity, reproducibility and harmonization. Duration of the internship: 3 months Minimum requirements What you'll bring to the role: - Candidates must be enrolled at a university/FH as Master/PhD student in Bioinformatics, Biomedical Sciences, Mathematics/Statistics or Pharmaceutical Sciences/Pharmacy. - Fluent in English (written and spoken) - The ideal candidate should have a very good knowledge of R and significant experience in developing R packages. Knowledge of NONMEM is a plus. Why consider Novartis: 750 million. That's how many lives our products touch. And while we're proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people's live ? We believe the answers are found when curious, courageous and collaborative people like you are empowered to as new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

05.02.2020

Novartis AG

Software Engineering Manager

  • Novartis AG

  • 4051Basel

  • 05.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288309BRPosition TitleSoftware Engineering ManagerApply to Job Job Description 6,000 people dedicated to discovery - 6 research campuses across the globe. Our research is passionate about discovering innovative new drugs that will change the practice of medicine. Novartis Institutes for BioMedical (NIBR) is the global pharmaceutical research organization of Novartis. We have an open and entrepreneurial culture, encouraging collaboration to make effective therapies As a Software Engineering Manager within the Software Engineering department, your role is to lead a team (~8 internal employees) who are responsible for ensuring the highest quality in software design, engineering, and architecture. You are a role model of Novartis Values & Behaviors: you care about patients, focus on what matters most, dare to challenge the status quo & experiment, take smart risks and always put your team before self. You are an inspiration to the associates who work with you. You engage others in our shared purpose and connect associates’ work with the shared purpose. You ensure you have the right people on your team who live up to our ethics, Values & Behaviors, leadership and culture expectations. You hold people to account and take action when performance and behaviors are not reaching our aspiration. You foster a learning culture within your teams. You are a learner, not a knower, and you are genuinely curious and open-minded. You empower and support others, you create clear accountability, and you remove obstacles for your team. You spend time mentoring and coaching team members. You are always clear, present and focused. You ask for feedback, you make it safe to give you feedback, and you are always looking for ways to improve yourself. Responsibilities Include but are not limited to: • Ensuring common process, standards and tools around software engineering are established and followed by their team (for ex: SDLC) • Leading all people management aspects of a local software engineering team. • Helping the product and software engineering planning and development process run smoothly. • Ensuring an engaged, innovative, and inspiring working environment in the department by motivating, challenging, and coaching employees towards growth. • Participating in personnel management practices regarding recruitment and selection, adequate staffing, performance appraisals, education and training, and management development. Minimum requirements What you will bring to this role: • BS/MS in Computer Science, Informatics or similar, or equivalent practical experience • Minimum 7 years of hands-on software development experience with a minimum of 3 years in a managerial role and 3 years with cloud and SaaS (Software as a Service) based solutions • Experience developing, implementing and supporting large-scale, highly scalable, highly available, data-driven software and cloud products in enterprise environments • Proficiency with a broad mix of software engineering frameworks, tools, and technologies including web application development and web services, traditional and NoSQL databases, distributed and cloud computing, data visualization, DevOps tools and processes, and more • Successful practical experience with Agile and Lean methodologies and with creating a strong DevOps culture • Strong organizational, problem-solving, and influencing skills and demonstrated track record of exceptional teamwork as well as excellent interpersonal, communication, and presentation skills Desirable Requirements: • Passion for innovating with data and digital at scale, applying modern technologies to large and complex problems, and creating measurable business value • Obsessive attention to detail, deep empathy for the end-user, and passion for the user experience & proven track record of successfully implementing quantitative, data-driven products in enterprise environments • Experience with pharmaceutical R&D and good understanding of scientific applications (but not necessarily science itself) • Working knowledge of German or French a plus but not required • Ability to travel 25% Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

05.02.2020

Novartis AG

Scientific Product Line Manager - Analysis and Reporting

  • Novartis AG

  • 4051Basel

  • 05.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288327BRPosition TitleScientific Product Line Manager – Analysis and ReportingApply to Job Job Description 6,000 scientists and physicians around the world use our data & systems to reimagine medicine and create therapies that save lives. Our research is focused on discovering innovative new drugs that will change the practice of medicine. Novartis Institutes for BioMedical (NIBR) is the global pharmaceutical research organization of Novartis. We have an open and entrepreneurial culture, encouraging collaboration to make effective therapies. At NIBR, our mission is to discover innovative medicines that treat disease and human health. To do that, our scientists need cutting-edge, state-of-the-art computing systems. With NIBR Informatics (NX), NIBR is making a strategic investment into informatics capabilities and is positioning itself to deliver the systems and services that are critical to the future of drug discovery. The Information Products and Data Sciences (IPDS) group in NX is driven to maximize the impact and value to NIBR of software and data. We deliver powerful, functional, beautiful, and integrated software solutions that create a frictionless user experience. Our organization is here to build and apply excellence in product and data management to further Novartis drug discovery. As the Analysis and Reporting Scientific Product Line Manager, you will develop and continually update a vision for a group of scientific software products that support data analysis and reporting for NIBR drug discovery. Working in collaboration with other Product Line Managers, your team will contribute to an integrated product suite. You will mentor and manage a small group of product managers who share this vision with you. You will define the standard for excellence in product management in our organization and synthesize that with your knowledge of drug discovery to create or license software that enhances and helps drive NIBR science. You will prioritize product roadmaps and direct development resources to maximize value to NIBR, and will define how we measure product success and value delivery. In this role, you will identify new product opportunities, deliver consistent, stable product operations, and meet all security, stability, usability, and performance and sustainability requirements. You will evangelize your product line, give product demos, and show the impact of your product line on NIBR science. Responsibilities include but are a not limited to • Develop a vision and roadmap for your product line, Analysis and Reporting • Manage a small team of product managers • Assess product development sprints, outcomes, and enhancement opportunities. • Achieve product line success and value metrics • Manage resources among product teams • May manage a product yourself • Establish excellence in product management practice Minimum requirements What you will bring to this role: • Minimum Bachelor’s degree in biology, chemistry, or a related scientific field. PhD preferred. • A Minimum of 3 years experience in product management in a complex matrix environment along with experience with Agile software development • Minimum of 5 years’ experience in drug discovery or a core supporting scientific field. • Proven experience as a mentor and team player with the ability to develop and promote a shared vision • A clear and visible set values and demonstrated integrity • Quantitative skills and the ability to use data and metrics to inform decisions Additional required core skills and capabilities: • Outstanding communication skills • Proven ability to execute consistently, rapidly, and effectively • Ability to travel 10% Additional - Leadership / Management Know-How As a Scientific Product Line Manager, you’ll help your direct reports succeed in their jobs, manage what they’re working on, and help them realize their career development goals. Removing obstacles and supporting your team members to prosper and grow will be an important aspect of your role. You will act as a mentor and role model in our organization, seeking, managing and retaining talent. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

05.02.2020

Novartis AG

IT Portfolio Planning Lead

  • Novartis AG

  • 4040Basel

  • 05.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288311BRPosition TitleIT Portfolio Planning LeadApply to Job Job Description 6,000 scientists and physicians around the world use our data & systems to reimagine medicine and create therapies that save lives. At NIBR, our mission is to discover innovative medicines that treat disease and human health. To do that, our scientists need cutting-edge, state-of-the-art computing systems. With NIBR Informatics (NX), NIBR is making a strategic investment into informatics capabilities and is positioning itself to deliver the systems and services that are critical to the future of drug discovery. You will enable NX to realize its highest value through a fully integrated portfolio. Within NX, the NOE department is accountable for helping NX deliver the highest value within a reasonable cost. NOE is responsible for central management of NX’s budget and ensures that NX delivers on financial goals. It helps NX to define its single strategy and realize it through fully integrated portfolio. NOE supports product and service delivery through disciplined planning, delivery, monitoring and measurement of results. Key responsibilities: • Creates and operates Adaptive Portfolio Management process for NX Products, Services and strategic Programs. • Collaborates across NX teams to develop a Road-Mapping process as the main tool for long term planning of NX Portfolio. • Works side-by-side with Portfolio operations to deploy, operate and continuously evolve processes, forums, documentation & tools used in the process. • Facilitates resource prioritization and change management process related to Strategic programs and material changes in Portfolio • Support Business Planning by integration of budget and headcount constraints into Portfolio selection and commitments. • Conducts feasibility assessment of delivery for planned Portfolio outcomes. • Sets up lean processes that enable independent decisions of empowered teams, and that brings holistic view of Portfolio to NX and its Stakeholders • Leads deployment of tools that enable fast decision making based on high quality of data owned by NX teams. Minimum requirements What you will bring to this role: • Minimum Bachelor’s Degree in Technology or Life Sciences or equivalent experience • Proven success with implementation and operation of Product/ Program Planning processes in a Software Product organization. • Strong expertise in IT Portfolio management and Stakeholder management • Minimum five years of experience managing teams accountable for business outcomes in a direct management or Project/ Program management role • Excellent communication, influencing and facilitation skills Experience with various Portfolio management tools such as Clarity, Planview, Planisware • Self-starter, able to develop a strategy and plan and execute from broad high-level objectives. • Able to deliver in matrix environments with high level of change. • Formal training in Project/ Program and Portfolio management (PMP Certified a plus) • Ability to travel 25% or less Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.02.2020

Novartis AG

Head Novartis Digital Patient Recruitment, CoE

  • Novartis AG

  • 4051Basel

  • 03.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288021BRPosition TitleHead Novartis Digital Patient Recruitment, CoEApply to Job Job Description 600 clinical trials - Novartis runs nearly double the number of clinical trials of any other pharmaceutical company. We have an unparalleled need for patients - at least 25,000 patients every year. Over 70% of those trials are late – mostly because we can’t find enough patients. But at the same time, 85% of patients say that they don’t know what their options are to participate in a clinical trial. This is a travesty – for Novartis and the patients who are waiting for our medicines or are looking for ways to contribute to helping those afflicted by disease. Come help us solve this problem using data, digital and social media – you can be instrumental in bringing hope and making an impact for patients. Your responsibilities will include: • Partner with Clinical Operations and Therapeutic/Development Units across Novartis to prospectively develop overarching strategy for digital recruitment, including overall approach in delivering effective digital clinical recruitment solutions • Evangelize the methodology, prove return on investment and manage stakeholder engagement at the highest levels of Novartis leadership • Provide thought-leader level knowledge and implant this across the organization to enhance awareness, uptake, and expertise in digital recruiting methodologies • Oversee and manage the Novartis Digital Recruitment Center-of-Excellence, comprised of a variety of strategic, technical and operational roles that support the enterprise with NDR activities. Measure performance and adapt CoE as needed • Oversee all NDR activities to develop a unified successful digital recruitment platform to position Novartis as an industry leader in this space [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Demonstrated experience in clinical-trial patient recruitment and/or digital recruitment methods • Successful and demonstrated experience in complex project management including budget • Demonstrated experience leading or managing within a cross-functional team, in a matrixed environment • Ideally, Experience operating as part of senior drug development leadership teams • Ideally, 10+ years of relevant experience in leadership clinical operations, patient recruitment and delivery, including awareness and understanding of rules and regulations globally WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitDATA & DIGITAL GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.02.2020

Novartis AG

Medical Device Expert Human Factors

  • Novartis AG

  • 4040Basel

  • 03.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID286438BRPosition TitleMedical Device Expert Human FactorsApply to Job Job Description 3 is the maximum number of steps that a user accepts to do when using an injection device! Designing simple devices is key to our success! To support the medical device development team we are seeking a Human Factors Device Manager to lead human factors activities in developing medical devices/combination products and apps, from early concept phase through to late phase development. This position is part of multidisciplinary and international teams, spanning across multiple projects, with human factors engineering being a key element for success. Depending on skillset and seniority level are hiring on either Device Expert II or Device Manager I level. Major responsibilities • Perform Human Factors activities on assigned projects • Lead the activities necessary for issuing the Human Factors deliverables (User profile, user capabilities, known use problems, complaints, task analysis, summary report…) • Support the development of user requirements and their translation into design inputs based on user capabilities • Support risk management activities such as the establishment of a risk management plan, identification of use-related hazards, development of a use-related risk analysis • Conduct formative and summative use evaluations • Compile human factors challenges and risks and provide design recommendations to be presented to the project team • Develop labeling and instructional materials • Support the development of Human Factors best practice, apply Human Factors best practice and share lessons learned • Support the development of standard operating procedures, work procedures, document templates and general guidance for the application of HFE in device development • Contribute to publications, presentations and patents Minimum requirements -Minimum: BS/MS or equivalent Desirable: Advanced degree in Human Factors/Ergonomics/User Interface/Engineering design or relevant discipline -Good knowledge of English (oral and written) -Desirable knowledge of site language -Successfully demonstrated 1-3 years’ experience in medical device or pharma industry or equivalent -Successfully demonstrated expertise in a specific area. -Thorough understanding of development processes in a specific function and some knowledge of related basic regulations -Good knowledge of software and computer tools. -Ability to work in team. -Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies. -Good communication skills. Good presentation skills and scientific/technical writing skills. May require up to 15% travel WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.02.2020

Novartis AG

Global Medical Affairs Director Cardio Renal Metabolic

  • Novartis AG

  • 4040Basel

  • 03.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID286721BRPosition TitleGlobal Medical Affairs Director Cardio Renal MetabolicApply to Job Job Description 50 Million! That is the number of how many patients with atherosclerotic cardiovascular disease worldwide do not achieve LDL-C lowering goals and remain at increased risk despite being on current standard of care. As part of Novartis, you are committed to reimagine medicine and be part of a remarkable team that shares the vision to transform clinical practice for patients with cardiovascular disease. You will also realize your potential while interacting with a outstanding employee community, working side by side with talented individuals and collaborating with the most respected academic institutions. Some of the best leaders in the industry will inspire you. This is a role waiting for you to put your own stamp on it. As our Global Medical Affairs (GMA) Director, you will be responsible for providing medical and scientific leadership into medical brand teams and other brand related functions from pre-launch through the whole life cycle of the compound. You will support the Global Brand Medical Director (GBMD) in the execution of GMA activities in alignment with GMA& Health Economics and Outcomes Research (HEOR) functions. Your responsibilities will include: • For the assigned Medical Affairs studies (Phase IIIB-IV, PMS, observational studies without regulatory impact) within program/brand, provide medical scientific input and delivery when appropriate. • Serve as a disease area scientific and medical expert for internal customers/stakeholders, e.g., GCT, Scientific Review Committee, research, exploratory development, device development, Marketing, Novartis local medical organizations, and other line functions within GMA and external customers e.g., Key Opinion Leaders (KOLs) and patient advocacy groups • Build together with the GBMD/Portfolio GBMD a highly influential medical and scientifically based platform. • Provide medical scientific input for the assigned program/brand(s) to co-develop with the appropriate functions an integrated Product Strategy (IPS), MA strategy and related MA plan as well as develop the medical affairs section of the clinical development plan. • Provide guidance to CPOs related to their MA study program; review, approve and follow up on local MA studies • Execute with the GMA team the global scientific communication plan Minimum requirements What you’ll bring to the role: • PhD with unique knowledge for successful clinical program development and execution, with ≥ 3 years of clinical research experience required OR • MD with specialty with board certification or equivalent, with ≥ 3 years of clinical research experience required • Medical Affairs and/or Market access experience • Medical and/or scientific expertise within disease area required and/or experience in having launched a vaccine • Experience in having launched a medication in a regional/global market • Demonstrated ability to establish strong scientific partnership with key investigators in assigned TA, academic institutions and scientific societies • Fluent English (Oral and Written) • Advanced medical/scientific writing and communication skills. • Strong track record of collaboration in a matrix environment WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGLOBAL MEDICAL AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.02.2020

Novartis AG

Regulatory CMC Portfolio Head - Biologics

  • Novartis AG

  • 4051Basel

  • 03.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID276425BRPosition TitleRegulatory CMC Portfolio Head - BiologicsApply to Job Job Description 200+ projects in development. 20 major approvals. 20 major submissions. And that’s just in 2018. This is your chance to help reimagine medicine in 2019. Novartis is looking for dedicated individuals to join our Global Regulatory Affairs team and contribute to developing our superlative pipeline of drugs and biologics into innovative therapies for our patients worldwide. And it all starts with you. Your interest, your talent, your initiative. Take the first step by looking at our track record of amazing accomplishments on behalf of our patients. Novartis employees have enjoyed long, rewarding careers working with colleagues around the world via flexible, family friendly arrangements. Read on for details about the role and how you can join a world-class organization at the forefront of the industry and how you can further your career. • In your role, you will lead a team of associates to establish and drive strategic and operational global CMC regulatory direction and documentation for a portfolio of projects/products covering development, registration and approval/post approval activities. You will energize associates around purpose and impact and champion a culture of ongoing learning and development. Further, you will align with stakeholders to achieve mutually beneficial outcomes to meet patient and business objectives. Your responsibilities include, but are not limited to: • Lead a team of associates to establish and drive strategic and operational global CMC regulatory direction and documentation for a portfolio of projects/products covering development, registration and approval/post approval activities. Energize associates around purpose and impact and champion a culture of ongoing learning and development. Align with stakeholders to achieve mutually beneficial outcomes to meet patient and business objectives. • As a member of the Global RA CMC Biologics leadership team, contribute to defining the strategic direction of the unit. Ensure robust regulatory strategies are developed and implemented to support the portfolio leading to timely Health Authority approvals. • Monitor regulatory trends and ensure continuous improvement related to Health Authority regulations, guidelines and feedback to ensure high quality and compliant regulatory dossiers are prepared. • Support the team in initiating and leading Health Authority interactions and negotiations. Support the team in initiating and leading Health Authority interactions and negotiations. • Recruit and develop associates ensuring the required level of knowledge and skills, identifying potential competency gaps. Identify talent and development opportunities; coach and mentor associates and create an engaged work culture. Minimum requirements What you’ll bring to the role: • Education: Science Degree (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent. Desirable: Advanced Science Degree • 10 years in regulatory preferred, and/or experience in pharmaceutical industry, experience in biologics. • Excellence in influencing people, negotiation and communication skills. • Strong leadership skills demonstrated by successfully leading a group or team (directly or indirectly), inspiring innovative thinking. • Excellent knowledge/experience in global regulatory submission and approval processes with broad knowledge of cGMPs and guidelines as they relate to regulatory CMC. • Strong interpersonal, organizational, presentation and problem solving skills and ability to develop individuals to accomplish goals through coaching, mentoring and timely feedback. 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? Why consider Novartis? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitREG AFFAIRS GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.02.2020

Novartis AG

Global Head Policies, Pricing-Value-Access

  • Novartis AG

  • 4040Basel

  • 03.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288043BRPosition TitleGlobal Head Policies, Pricing-Value-AccessApply to Job Job Description 8! The number of launches planned over the next 2 years. Your business acumen and communications mastery will help the world understand what these medicines do, why they matter and how Novartis is striving to reimagine medicine. Creating and advancing Novartis policy strategic framework related to the pricing, value and access of medicines that support Novartis's advocacy portfolio and which create competitive advantages while ensuring that these initiatives align with the overall mission, vision and values of Novartis. Your responsibilities will include: • Operate as an enterprise leader to drive strategic thought leadership with Novartis global leaders, regions, countries and business franchises, as well as, influential external organizations to achieve measurable impact to Novartis business objectives • As a member of Global PA Leadership Team, will build and leverage well-developed network to keep leadership informed of priority pricing, value and access issues and opportunities to expand and protect portfolio • Lead Novartis internal Pricing, Value and Access Policy team and cross-divisional practice group to develop focus, strategic and proactive plans to shape external healthcare policy positions to advance the interest of Novartis • Develop stakeholder communication policy content and narratives and prepare Novartis associates from all levels (top management to country level) to engage with impact advocacy efforts, accomplish stakeholder understanding of company positions and rationale, and increase company reputation. • Supervise and motivate a team of trained professionals, allowing and encouraging growth and independence, and leveraging their skills in a way that will increase the visibility and credibility of the function Minimum requirements What you’ll bring to the role: • Masters/PhD, e.g. in law, public health, health policy or business administration, or PhD desirable • 10+ years in the pharma industry, including several years of operational and strategic roles in Pricing, Market Access HEOR or related positions • Experience in policy relates roles, ideally in both Industry and consulting • Strategic mindset with exceptional interpersonal and partnering skills, and proven ability to lead with high impact in a matrix organization Desirable requirements: • Experience in a policy setting body such as OECD, WHO, World Bank • People leadership experience WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitNOVARTIS CORPORATE AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaCommunications & Public AffairsJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.02.2020

Novartis AG

Solution Delivery Manager - Robotic Cognitive Automation

  • Novartis AG

  • 4051Basel

  • 03.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID288186BRPosition TitleSolution Delivery Manager – Robotic Cognitive AutomationApply to Job Job Description 130+ bots live and many in the pipeline! An innovative multidisciplinary IT team in Novartis, you will be part of the integral talent in collaborative innovative and agile teams that experiment, rapidly incubate and establish to scale digital platforms that deliver value to Novartis in areas like Process Automation, Cognitive Computing (AI, ML), Natural Language Processing, etc. Position purpose Manage the planning, design and build of Robotic Cognitive Automation (RCA) solutions, based on user requirements / problem statement, while meeting quality and performance requirements and technical constraints. Manage the scheduling and deployment of RCA solutions across multiple countries and/or functions. Responsibilities: Drive Robotic Cognitive Automation (RCA) solutions with the Business and IT teams: • Organize solution design, development and deployment efforts for projects by compiling the required resources and assigning responsibilities according to a defined time schedule • Ensure that detailed designs match high level designs and are traceable to requirements in functional specification • Ensure designs produced adhere to architectural roadmap and support the development, execution and operations of solutions • Ensure the overall user experience is taken into account when designing and deploying new solutions and services • Ensure that all work is delivered to agreed time, cost and quality constraints • Initiate solution testing to ensure they meet quality standards • Establish standardized design and development processes to enable cost effective delivery • Authorize and conduct service handover and lead the go-live authorization discussions with the other work streams • Ensure that all release and deployment packages can be tracked, installed, tested, verified and backed out (if required) • Take accountability to ensure adherence with Security and Compliance policies and procedures within Solution Delivery scope Minimum requirements • Masters in Computer Science/AI or equivalent areas • Fluent in English, other languages beneficial • Minimum of 5 years of product/delivery management or equivalent experience • Proven track record of managing all aspects of a successful product / service delivery throughout its lifecycle • Solid technical background with understanding and/or hands-on experience in software/web development • Proven ability to identify technology options and drive decision-making that balances business and technical requirements • Strong problem solving skills and willingness to roll up one’s sleeves to get the job done • Skilled at working effectively with cross functional teams in a matrix organization • Excellent written and verbal communication skills • Experience working in an agile environment, delivering via incremental releases WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionNBSBusiness UnitIT NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.02.2020

Novartis AG

Process Expert (80-100%)

  • Novartis AG

  • 4051Basel

  • 03.02.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID286989BRPosition TitleProcess Expert (80-100%)Apply to Job Job Description 105,000 unique individuals work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose: to Reimagine Medicine for millions of patients around the world! Your responsibilities will include, but are not limited to: • The Process Expert (PE) supports the Production Unit (PU) in providing front line expert support for all Bioprocess-specific issues to production: Provide with scientific and biotechnological expertise process performance and data evaluation • Evaluate and implement production strategies/new technologies and support improvement/OPEX initiatives in collaboration with MST and quality unit. • Perform deviation investigations and process changes within the PU. Support biotechnological process transfers and process validations in collaboration with MST. • Ensure process lay-out and process adaptations in the PU and troubleshooting of process-specific issues. • Prepare, support and follow-up of internal and external audits for own area. Act as subject matter expert for process related Health Authority questions. Minimum requirements What you’ll bring to the role: • MSc. or PhD in Biotechnology, Pharmaceutical Technology, Chemistry, Pharmacy or equivalent scientific degree. • Excellent knowledge of upstream processes and technologies for cell cultivation. Experience in mammalian cell culture at pilot scale preferred. • Proven process understanding (Biotech, Pharma, GMP, Regulatory aspects). • Excellent knowledge of GMP regulations (proven hands on experience in Deviation handling, CAPA management, SOP writing) and proven track record within GMP environment preferably in Biotechnology. • Fluent English (oral and written) and fluent German Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNovartis Technical OperationsBusiness UnitNTO BIOTECHNOLOGYLocationSchweizSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaTechnische OperationenJob TypeVollzeitEmployment TypeUnbefristetShift WorkNein Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.02.2020

Novartis AG

Digital Recruitment Strategist

  • Novartis AG

  • 4040Basel

  • 03.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID287867BRPosition TitleDigital Recruitment StrategistApply to Job Job Description 600 clinical trials - Novartis runs nearly double the number of clinical trials of any other pharmaceutical company. We have an unparalleled need for patients - at least 25,000 patients every year. Over 70% of those trials are late – mostly because we can’t find enough patients. But at the same time, 85% of patients say that they don’t know what their options are to participate in a clinical trial. This is a travesty – for Novartis and the patients who are waiting for our medicines or are looking for ways to contribute to helping those afflicted by disease. Come help us solve this problem using data, digital and social media – you can be instrumental in bringing hope and making an impact for patients. As our Digital Recruitment Strategist you are an Enterprise leader, who is accountable for setting and delivering upon a best-in-class digital recruitment strategy for key clinical trials. These recruitment strategies will include digital media, advocacy group presence and partnerships, inventive/unique approaches, and social media – both established (facebook) and emerging (snapchat, wechat, future undefined).At the same time, you will be helping to define a ‘first in class’ model that does not exist in the industry today, in collaboration with the NDR CoE Head. You will be responsible for working with many partners across Novartis to coordinate approaches and bring break-through results for Novartis assets during the drug development process. Your responsibilities will include: • Accountable for setting and delivering on a best-in-class digital recruiting strategy, for supported studies • Partner with program/trial teams to develop overarching strategy for digital recruitment, including communications approach, channel strategy, budget • Oversee development and implementation of the Digital Recruitment Plan for assigned projects and studies; maintain oversight post-implementation to troubleshoot issues and adapt ongoing strategy based on performance feedback • Ambassador to internal NIBR/GDD development units to craft therapeutic area approaches and over-arching recruitment strategy by indication and key target patient indications • Responsible for therapy-are and patient level insights generation, via work with internal Novartis groups and external agencies/patient groups as appropriate [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Demonstrated experience in clinical-trial patient recruitment and/or digital recruitment methods • Successful and proven experience in complex project and program management including budget • Bachelors or equivalent 4-year university degree required in related area (i.e., science, clinical, digital, marketing); Masters or higher preferred • Substantial (5+ years) experience in one of the following (preferably multiple): Clinical trial recruitment in Development operations, Digital media creative and execution (e.g., agency), Management of external partners who deliver digital recruitment strategies WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitDATA & DIGITAL GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

03.02.2020

Novartis AG

Scientific Associate II - Biologics (80-100% )

  • Novartis AG

  • 4051Basel

  • 03.02.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID287006BRPosition TitleScientific Associate II - Biologics (80-100%*)Apply to Job Job Description 6500! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. We are looking for a motivated and curious scientist and strong team player to join our team at the research and development interface: and work on the Early Screening of Cell Lines and in mammalian cell cultivation and recombinant cell line generation. Your responsibilities will include, but are not limited to: • Generation of recombinant cell lines in various mammalian host cell backgrounds to enable therapeutic protein discovery and development • Generation of production Chinese Hamster Ovary (CHO) cell lines that are the basis for Biologics manufacturing • Small scale expression testing by transient transfection of mammalian cells with subsequent analysis using Western Blot, ELISA, flow cytometry and other assays • Interaction with Biologics research and development project teams and presentation of results in team meetings • Reporting of results into electronic lab notebooks compliant with Research and Development non-GMP quality standards Minimum requirements What you’ll bring to the role: • Background in biotechnology, cell biology, and/or Biologics drug discovery (BSc, MS or apprenticeship with 3+ years of professional experience) • Strong technical expertise in mammalian cell cultivation (small and mid scale) and recombinant cell line generation • Background in transient transfection of mammalian cells • Strong technical expertise in flow-cytometric analysis of mammalian cells • Fluency in English is mandatory, fluency in German a plus • Strong team player attitude with excellent communication & interpersonal skills and capable of working semi-independently or as part of a cross-functional team Desirable requirements: • Technical expertise with FACS-based single cell sorting of mammalian cells • Strong background in molecular biology Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNIBRBusiness UnitBIOTHERAPEUTIC AND ANALYTICAL TECHNOLOGIES - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

31.01.2020

Novartis AG

Digital Content Strategist (80-100% )

  • Novartis AG

  • 4051Basel

  • 31.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID287571BRPosition TitleDigital Content Strategist (80-100%*)Apply to Job Job Description 600 clinical trials! Novartis runs nearly double the number of clinical trials of any other pharmaceutical company. At least 25,000 patients every year. Over 70% of those trials are late – mostly because we can’t find enough patients. But at the same time, 85% of patients say that they don’t know what their options are to participate in a clinical trial. This is a travesty – for Novartis and the patients who are waiting for our medicines or are looking for ways to contribute to helping those afflicted by disease. Come help us solve this problem using data, digital and social media – you can be instrumental in bringing hope and making an impact for patients. Position purpose: The Digital Recruitment Content Strategist is responsible for the content strategy and implementation for digital patient recruiting from creation to retirement across NDR assets, standards management and standard methodologies. This includes oversight and management of internal and external partners (agencies) to develop and deliver high quality content, as well as adapting successful communication strategies throughout the lifecycle of a trial supported by Novartis Digital Recruitment (NDR). The Digital Recruitment Content Expert is accountable for high quality and bespoke content that will be used on publicly visible media for Novartis overall (websites, social channels, etc.), including fit-for-purpose to various patient populations, as well as Novartis’ reputation! Major accountabilities •Direction on content strategy and implementation to support digital patient recruiting supported by NDR, and tracking use throughout the study lifecycle, being responsible and accountable for all the content assets. •Work independently and/or with external agencies to co-create content related to Novartis digital patient recruitment, including but not limited to text, ads, data elements, social and multimedia •Accountable for driving external partners and content produced that will be utilized by NDR and Novartis enterprise level external communications. •Update content strategy for above-brand digital presence and for each study in the NDR platforms •Work with study teams, in partnership with NDR Digital Recruitment Strategist, to validate approaches and ensure team content alignment and approval •Develop and maintain content library, templates and approaches/methodologies for NDR materials. •Develop content approaches across studies, projects, and indications – per portfolio needs •Drive consistent, coherent and compliant branding connected to Novartis standards. Input and feedback on potential improvements as required •Maintain the NDR Playbook content: responsible for ensuring regular updates and continued relevance of the content •Owner and manager of NDR Common Standards related to content, and consistency across all campaigns as meaningful •Develop end of campaign and insights reports on study or indication levels to ensure best practices are captured and carried forward •As needed, work with other internal and external patient communications and/or advocacy teams to further develop and generate best practices in patient-facing communications Minimum requirements • Masters or PhD in Communications, Journalism, Marketing, Public Relations or relevant field • Very high proficiency with oral and written English. • 8+ years proven experience planning, creating, launching, measuring, prioritizing, and maintaining content on consumer websites for marketing purposes, including 5+ years of content strategy and/or multichannel marketing experience. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitCOMMS GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaCommunications & Public AffairsJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

31.01.2020

Novartis AG

Head of Quality Engineering

  • Novartis AG

  • 4051Basel

  • 31.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID285053BRPosition TitleHead of Quality EngineeringApply to Job Job Description 6,000 people dedicated to discovery - 6 research campuses across the globe. Our research is passionate about discovering innovative new drugs that will change the practice of medicine. Novartis Institutes for BioMedical (NIBR) is the global pharmaceutical research organization of Novartis. We have an open and entrepreneurial culture, encouraging collaboration to make effective therapies. As Head of the Quality Engineering department, your role is to lead a team of high performing quality engineers with a focus on test automation and ensuring a high software quality standard across our portfolio of applications. Responsibilities include but are not limited to: •Serve on the Engineering Leadership Team to define + ensure common process, standards and tools around software quality engineering are established and followed by their teams as well as •Drive for high degrees of test automation and code coverage across our products. •Working hands on as a quality engineer •Participate in personnel management practices regarding recruitment and selection, adequate staffing, performance appraisals, education and training, and management development. •Ensure an engaged, innovative, and inspiring working environment in the department by motivating, challenging, and coaching employees towards growth. Minimum requirements What you will bring to this role: •BS/MS in Computer Science, Informatics or similar, or equivalent practical experience •10 years minimum of hands-on software development experience with 3 years minimum in a managerial role and 3 years minimum with cloud and SaaS (Software as a Service) based solutions •Prior experience as a software engineer or QA as well as leading technical teams •Successful practical experience with Agile and Lean methodologies and knowledge of DevOps + Cloud technologies •Strong organizational, problem-solving, and influencing skills with demonstrated track record of exceptional teamwork as well as excellent interpersonal, communication, and presentation skills •Working knowledge of German or French a plus •Ability to travel 25% WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

31.01.2020

Novartis AG

Real World Evidence Executive Director, Ophthalmology (80-100% )

  • Novartis AG

  • 4051Basel

  • 31.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID287884BRPosition TitleReal World Evidence Executive Director, Ophthalmology (80-100%*)Apply to Job Job Description 200 million patients worldwide are treated with Novartis ophthalmic products. Our Ophthalmology Franchise is reimagining what’s possible by bringing life-altering treatments to patients with visual impairments and blindness. RWE role based in Novartis’ Headquarter, will have the mission of ensuring those patients can access treatment across the Globe. Your responsibilities will include: • Provide thought-leadership and enable cross-functional teams (V&AT, GMAT, GPT) in becoming leaders in utilization and generation of RWE and enabling them to leverage RWE in innovative and advanced ways. • Create and implement uniform excellence standards across franchises for development and reporting of RWE. • Focus on priority disease areas and gaps, responsible for the development of a sustainable innovative and scientifically robust Real World Evidence (RWE) strategy within the Business Franchise. • Development and successful implementation of franchise RWE plan in collaboration with involved key functions such as Medical, HEOR, Market Access etc. • Work closely with franchises in regions and CPOs to enable capability building and sharing of best practices across geographies. Work with regions and CPOs to develop blueprints for organizing effective local RWE teams in a franchise. • This role will be a member of the leadership teams in the Center of Excellence for Real World Evidence, the Franchise Patient Access Leadership Team, and also the Franchise Medical Affairs Leadership Team, and build strong partnerships with both global and local Franchise and Function heads. [#video#https://www.youtube-noccokie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • 8/10+ years relevant experience acquired at pharmaceutical companies, academia, healthcare provider / Payer / HTA, or relevant consultancy companies • Deep understanding of Medical Affairs, HEOR, Safety or related disciplines to generate value evidence from retrospective and prospective studies. Desirably, an active external network in area of RWE generation. • Very strong understanding of drug development and commercial disciplines, demonstrated ability to identify key evidence needs for Commercial, Market access, Medical, Safety, Regulatory stakeholders and lead a team towards building the required insights • Considerable experience in planning, creation, and analysis of real-world data, from both prospective and retrospective studies with a proven success record in this field • Experienced and with a strong knowledge of research methodology and statistical methods in the field of prospective clinical data analysis • Strong organizational, interpersonal and influencing skills • Previous work and leadership in international and multidisciplinary drug development and product teams • Ability to communicate effectively and motivate team alongside having a persuasive and credible presentation style at all levels of organization WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarket AccessJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

31.01.2020

Novartis AG

Global HEOR Director, Ophthalmology (80-100% )

  • Novartis AG

  • 4040Basel

  • 31.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID287886BRPosition TitleGlobal HEOR Director, Ophthalmology (80-100%*)Apply to Job Job Description 200 million patients worldwide are treated with Novartis ophthalmic products. Our Ophthalmology Franchise is reimagining what’s possible by bringing life-altering treatments to patients with visual impairments and blindness. HEOR Director role based in Novartis’ Headquarter, will have the mission of ensuring those patients can access treatment across the Globe. Your responsibilities will include: • Generate evidence supporting the value of Novartis brands in order to achieve optimal pricing and market access (reimbursement and formulary listing), as well as support other commercialization activities. • Execute Health Economics and Outcomes Research (HE&OR) strategies that demonstrate overall product value. • Develop and integrate parameters necessary to demonstrate clinical, economic, and humanistic product value to payers and other decision-makers into clinical trial programs (Registration and Brand Optimization Studies). • Lead the efficient and timely development of HE&OR deliverables (global value dossiers, publications, and health economic models). • Represent HE&OR on cross-functional teams including: International Project Teams, International Clinical Teams, Brand Teams, and Value Demonstration Teams. • Ensure of HE&OR strategy is aligned with Commercial and Market Access strategies and prepare HE&OR section of clinical development plans (CDPs). • Coordinate HE&OR research strategies with Country Pharma Organization (CPOs) including integration of CPO HE&OR needs into clinical development program. • Effectively communicate research findings internally and externally. [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Undergraduate degree in a relevant scientific discipline plus graduate degree (Masters or PhD) in relevant discipline including health economics, epidemiology, health services research, biostatistics • English fluent • >2 years conducting health economic and outcomes research for pharmaceutical products in the pharma industry or experience in a closely related discipline within the pharma industry (e.g., clinical development, commercial, pricing) or with a contract research organization with demonstrated previous research accomplishments • Strong technical knowledge in HE&OR study methods coupled with understanding of Health Economics (HE) and outcomes research field, including key opinion leaders and leading academic researchers and consultants. • Awareness of sources of clinical information including disease epidemiology and treatment; formal training in a clinical science or basic physiology desirable WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarket AccessJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

30.01.2020

Novartis AG

Global Head Strategy & Change Management, Digital Commercial Execution

  • Novartis AG

  • 4040Basel

  • 30.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID287779BRPosition TitleGlobal Head Strategy & Change Management, Digital Commercial ExecutionApply to Job Job Description 30,000+ associates in Pharma and Oncology are focused on getting our medicines to the patients that need them while providing value added services to Healthcare Providers. Our Digital Commercial Execution team has been formed to provide digital programs and solutions at scale that will have significant impact on the success of the enterprise and that are implemented at scale across our Pharma and Oncology businesses. These solutions are relevant to millions of customers and applicable to more than 100,000 daily interactions with Healthcare Providers. Play a key role in a team that will build an industry leading, future-proofed foundation that will power commercial teams by putting data, digital, and artifical intelligence in practice. This strategic role will closely partner with the Head of Digital Commercial Execution to develop and deploy an industry-leading commercial data analytics platform for Pharma and Oncology that will improve the impact of our sales and marketing teams. You will support our commercial business units to move from data rich to delivering insights from data/digital to benefit our patients. Specifically as Head of Strategy and Change Management you will provide holistic support to the DCE governance board and team to ensure delivery against objectives and KPIs. Additionally you will be responsible for change management required for the success within the program and partner as necessary with the business to support change management locally. You will inspire the team with an entrepreneurial mindset and the courage to push for innovation. You will work in an agile fashion in a nimble program organization. You will be responsible but not limited to: • Portfolio Prioritization as business priorities evolve; • Secretary to the DCE Governance board • Refines Governance and Operating Model as product maturity evolves • Leads Program and Change Management in partnership with PBU and OBU leaders • Coordinates Value and Impact measurement • Manages Resourcing including overall budget and team resourcing operations (e.g rotations, etc) Minimum requirements • University Degree with specialty in pharmacy, medicine, or business • Fluent spoken & written English. Additional languages a plus. • Commercial experience in various roles across global, region, and local and across discplines (sales, marketing, etc) in pharmaceutical industry • Consulting experience and/or demonstrated similar capabiltiies internally • Experience working in a complex organization, building relationships and driving engagement • Previous experience and strong mindset in continuous improvement and change management; Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionCORPORATEBusiness UnitDIGITAL OFFICELocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaBD&L & Strategic PlanningJob TypeFull TimeEmployment TypeRegularShift WorkYes Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

30.01.2020

Novartis AG

Global Head of Foundational Processes, Digital Commercial Execution

  • Novartis AG

  • 4051Basel

  • 30.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID287675BRPosition TitleGlobal Head of Foundational Processes, Digital Commercial ExecutionApply to Job Job Description 30,000+ associates in Pharma and Oncology are focused on getting our medicines to the patients that need them while providing value added services to Healthcare Providers. Our Digital Commercial Execution team has been formed to provide digital programs and solutions at scale that will have significant impact on the success of the enterprise and that are implemented at scale across our Pharma and Oncology businesses. These solutions are relevant to millions of customers and applicable to more than 100,000 daily interactions with Healthcare Providers. Play a key role in a team that will build an industry leading, future-proofed foundation that will power commercial teams by putting data, digital, and artificial intelligence in practice. This strategic role will partner closely with the Head of Digital Commercial Execution to develop and deploy an industry-leading commercial data analytics platform for Pharma and Oncology that will improve the impact of our sales and marketing teams. You will support our commercial business units to move from data rich to delivering insights from data/digital to benefit our patients. As the Head of Foundational Processes you will establish, accelerate, maintain and coordinate a complex portfolio of business processes such as customer master data management (MDM), digital content management, call preparation, key account management, and more. Furthermore, you will establish best-in-class capabilities in process management and ensure the processes enable the creation and sustainable implementation of a portfolio of digital products that will be used in our commercial organization. You will inspire the team with an entrepreneurial mindset and the courage to push for innovation. Your responsibilities will include: • Identify and prioritize critical processes to enable the portfolio of products being developed by the Digital Commercial Execution (DCE) team • Consolidate business needs and ensure business process delivers against them • Lead a team of Global Process owners who ensure that each process is clearly defined, designed, documented and implemented. • Hold process owners accountable for identifying the core harmonized processes and local nuances required to be met • Understand and coordinate process interdependencies • Ensure blockages impeding processes or product teams are addressed • Lead organizational change management and application of continuous improvement principles • Provide business process subject matter expertise, ensure adherence to common standards and build an overall foundational process capability with strong business ownership • Maximize value and ensure feasibility at the intersection of business, customer/end-user, and technology – stakeholder management across these groups [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • University Degree with specialty in pharmacy, medicine, or business • Commercial experience in various roles across global, region, and local and across disciplines (sales, marketing, etc) in pharmaceutical industry • Demonstrated experience with business process definition, creation, and maintenance • Experience working on technical or analytical projects, with a deep understanding of customers • Expertise in organization dynamics and culture, ability to gain trust and confidence at all levels in the organization, leadership and project management experience in global initiatives. • Ability to influence at all levels of the organization in a matrixed environment • Previous experience and strong mindset with systems thinking, continuous improvement and change management • Entrepreneurial, agile, non-hierarchical mindset, constantly seeking better by gathering insights and using data feedback loops to iterate and re-invent, to better address the problems customers are trying to solve WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitDIGITAL OFFICELocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

30.01.2020

Novartis AG

Global HEOR Director, Cardio-Renal-Metabolic

  • Novartis AG

  • 4051Basel

  • 30.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID287799BRPosition TitleGlobal HEOR Director, Cardio-Renal-MetabolicApply to Job Job Description Decades of untapped unmet needs in the Cardio-Renal-Metabolic (CRM) space are waiting for your footprint and guidance! As part of the long-term CRM strategic and operational growth plan, this is an ideal opportunity to bring new innovative products to those in need. We seek to become the leading innovators in the CRM space by developing a transformative Precision Medicine specialty portfolio for areas of high-unmet medical need. Our new Global HEOR Director role based in Novartis’ Headquarter, in collaboration with a very diverse team, will provide, assess and bring life-saving drugs to patients globally! Your responsibilities will include: • Leadership and influencing relevant franchise cross functional teams from an HEOR point of view. Creating an innovative, data-driven disease area specific HEOR strategy: a. Creating HEOR publications & white papers (impact of emerging data, new mechanisms, new technologies, hypothesis generation) relevant to disease area strategy b. Works across development and commercial functions to support the creation of ‘real world data’ for key products in the disease area from early development to phase iv c. Facilitates identification, development and acceptance of novel development approaches and analytic data mining activities • Provides expert HEOR input and is accountable for influencing cross-functional teams, in particular: a. HEOR Disease story to support Patient Access Strategy, b. Clinical Development Plan(s) from an HEOR point of view within a specific disease area, including contribution to Business Development licensing evaluations and Novartis Institute for Biomedical Research (NIBR) PoC and sPoC plans c. New study endpoints for disease area relevant to payers and other non-traditional customers e. Innovative within and cross project data for use in (value for money) clinical & payer decision making Aim for five bullet points • Accountable for delivering disease specific HEOR activities and for building validated ‘ready to use’ protocols in medical and clinical development (key sections of IPS documents, Medical affairs plans, clinical protocols such as inclusion/ exclusion criteria, statistical methodology, statistical tables and graphs, etc.) • Provides expert HEOR input into due diligence assessments of potential licensing and acquisition projects and provide review of clinical due diligence reports including proposed clinical development plans Minimum requirements What you’ll bring to the role: • 8-10 years’ experience in the pharmaceutical industry in an HEOR setting with a strong track record of high impact HEOR publications and academic achievement • Ability to lead HEOR reputation for the Cardio, Renal Metabolism franchise in order to enable the most innovative scientific and operational HEOR inputs resulting into a competitive advantage and ensuring quick and differentiated HEOR evidence that exceed clinical, regulatory/market access requirements and patient needs • Strong track record of innovation on combination with a results driven mindset • Exceptional leadership and communication skills with the ability to influence effectively across senior matrix teams Desirable requirements: • Above country experience, ideally in global • A world class expert in Cardiology • Experience with vaccines WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarket AccessJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

30.01.2020

Novartis AG

Internship Pharmacometrics for Master or PhD students

  • Novartis AG

  • 4040Basel

  • 30.01.2020

  • Praktikumsstelle

Back to Previous Page Job ID287764BRPosition TitleInternship Pharmacometrics for Master or PhD studentsApply to Job Job Description 700! The number of days we can get therapies faster to patients applying Technology innovation. Your responsibilities will include: As intern you will work on your own statistics or pharmacometrics projects, under the guidance of senior-level quantitative scientists, to design and analyze clinical trials and/or perform relevant quantitative research. Various real-world problems will give you hands-on exposure to early and late phases of drug development across different therapeutic areas, including oncology, cardiology, immunology, neurology, ophthalmology, and respiratory care. Potential topics include disease progression modeling, PK/PD modeling, survival analysis, causal inference, Bayesian statistics, and/or machine learning and deep learning. Interns will also attend seminars and other activities to enhance their understanding of the drug development process. Further, there will be opportunities for you to present their project results to all quantitative scientists and other stakeholders. Duration: 3 months Minimum requirements What you'll bring to the role: - Candidates must be enrolled at a university/FH as Master/PhD student in Bioinformatics, Biomedical Sciences, Mathematics/Statistics or Pharmaceutical Sciences/Pharmacy. - English fluent in written and spoken - Ideal candidate should have a good familiarity with quantitative methods and/or modeling in one-two domains among the following: mathematical, statistical, biological, pharmacological. - Excellent oral and written communication skills and strong problem-solving skills. - Working knowledge R or SAS is preferred. - Some projects require a strong background in NONNEM, Monolix, Phyton and/or other software and languages. Why consider Novartis: 750 million. That's how many lives our products touch. And while we're proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people's live ? We believe the answers are found when curious, courageous and collaborative people like you are empowered to as new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Senior GDO Portfolio Analyst

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID287239BRPosition TitleSenior GDO Portfolio AnalystApply to Job Job Description 90,000 are the number of patients we touch every year with our innovative Clinical Trials. In Global Development Operations (GDO) we believe we have a unique opportunity to transform clinical operations through predictive data insights to accelerate the reach of our medicines to patients. As part of the Transformative Business Operations (TBO) team, be an actor of industry leading changes. As our Senior GDO Portfolio Analyst you will be accountable for leading the technical development, system integration and enhancement of our industry-first predictive risk identification platform – SENSE. Through this incredible lens, you will be at the heart of applied data science and analytical techniques, including explorative applications of machine learning, deep learning & artificial intelligence to translate data insights into operational insights & business intelligence. And all this in partnership with our Line Functions and across our full 800 clinical trial portfolio (Early, Full and Late Development). Your responsibilities will include: • Act as the SENSE technical lead for design, system integration and enhancement of predictive planning tools and supporting data science projects (i.e. reporting, data governance, transformative solutions). • Matrixed leadership of a team of operational/business and technical experts responsible for strategic technical guidance, process development, and workload prioritization • Primary lead for day-to-day operations within the SENSE Bridge (physical control room • Drive organizational decision-making through the utilization of advanced machine learning, and AI techniques which support early risk assessment and optimal GDO portfolio execution • Lead the translation of data insights into operational insights by working with relevant partners to scope data science requirements: needs identification, hypothesis generation, data discovery and methodology proposal • Drive the preparation of relevant data and prototype appropriate analytical models • Proactively identify risk/trends to enrich future portfolio model rule definitions and predictive analytics within the SENSE application [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Master degree in quantitative field like Data Science, Mathematics, Physics, Engineering, or related field required • High proficiency in English (oral and written) • 5+ years post-graduate experience in a multidisciplinary data & analytics environment or in research • Expert knowledge of advanced applied data science (machine learning, neural networks, etc.), mathematical modeling, computational, statistical and data mining techniques (regression, decision trees, clustering etc.) • Proficiency in R, Python, MLlib, TensorFlow, Matlab, SAS, SPSS or collection of equivalent data science packages and frameworks • Experience with User Experience (UX) design and Design Thinking • Experience in program planning and management skills including experience with project management methodology and tools (preferably Agile) • Strong communication skills both verbal and written, and ability to communicate analytical and technical content with clarity to non-experts • Result-driven achiever with demonstrated leadership with the ability to inspire others, build strong relationships with team members and key stakeholders • Raw inquisitiveness and intellectual curiosity, along with excellent problem-solving and quantitative skills, including the ability to break apart issues, identify root causes and recommend solutions • Self-motivated with a high degree of ownership and accountability for results WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Clinical Development Medical Director(CDMD) /Senior CDMD, Neuroscience

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID276428BRPosition TitleClinical Development Medical Director(CDMD) /Senior CDMD, NeuroscienceApply to Job Job Description 60! With a 60-year history in neuroscience, Novartis has brought innovative therapies to patients with e.g. Multiple Sclerosis, Alzheimer’s disease, Parkinson’s Disease, Epilepsy, Depression and Migraine. We have a world-class pipeline in neurodegeneration, neuro-inflammation, neuromuscular and psychiatric diseases. Our holistic R&D approach includes cutting edge molecules, innovative approaches to technology, biomarker and digital therapeutics to seek better solutions for patients. As a Clinical Development Medical Director (CDMD) / Senior CDMD, Neurology, you will join a dynamic team who are dedicated to developing treatments to slow the progression of degenerative orphan diseases including Huntington’s disease and Spinal Muscular Atrophy. Your role will be to lead and provide medical strategic input for clinical deliverables or clinical sections of such deliverables (e.g. study protocols, pediatric plan, clinical data review, safety updates, health authority responses, investigator brochures, submission dossiers, briefing books, etc.) for a program in early stage clinical development in Huntington’s disease and a more advanced program in spinal muscular atrophy. Your responsibilities will include: • Providing clinical leadership and medical strategic input for all clinical deliverables in the assigned project or section of a clinical program if applicable. Clinical deliverables may include clinical sections of individual protocols consistent with the Integrated Development Plans, clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications • Leading development of clinical sections of trial and program level regulatory documents (e.g., Investigator’s Brochures, briefing books, safety updates, submission dossiers, and responses to Health Authorities) • Driving execution of the section of the clinical program in partnership with global line functions, assigned Global Trial Directors, and regional/country medical associates if applicable • Supporting (Sr.) Global Program Clinical Head in ensuring overall safety of the molecule for the assigned section, acting as a core member of the Safety Management Team, and supporting overall program safety reporting (e.g., Periodic Safety Update Reports, Drug Safety Update Reports, and other safety related documents), in collaboration with Patient Safety • Supporting the Therapeutic Area Head (TAH) by providing medical input into Integrated Development Plans and CTP reviews and contributing/driving development of disease clinical standards for new disease areas. May take on other responsibilities as directed by the TAH • As a medical expert, supporting the (Sr.) Global Program Clinical Head or TAH in interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, data monitoring boards, advisory boards, patient advocacy groups), internal stakeholders (e.g., Clinical Trial Team, Research, Translational Medicine, Global Medical Affairs, Marketing, HE&OR), and internal decision boards Minimum requirements What you’ll bring to the role: • MD or equivalent medical degree required. Advanced knowledge and clinical training in neurology required, with Medical Board certification • Experience >7 years in late or early drug development for psychiatry and/or neurology, orphan indication or neurodegenerative disease experience preferred • Demonstrated ability to establish strong scientific partnership with key stakeholders • Thorough knowledge of GCP, clinical trial design, statistical analysis methodology, and regulatory/clinical development process • Demonstrated experience in data presentation and strong negotiation and diplomatic skills, experience with health authorities required The final level of hire will depend on the successful candidates level of expertise WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Real World Evidence Director, IHD (80-100%)

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID283936BRPosition TitleReal World Evidence Director, IHD (80-100%)Apply to Job Job Description 195 countries and thousands of patients worldwide need support to access new innovative treatments in Immunology, Hepatology and Dermatology (IHD)! With your expertise, we will systematically integrate access in how we research, develop and deliver new medicines globally. Be part of the team that is working on launching 6 potential blockbusters in the next 6 years. Your responsibilities will include: • To ensure a broad understanding of the value of RWE to the product value demonstration both globally and locally. Lead and ensure innovative, best-in-class evidence planning and creation, to improve value of key development projects, products, and businesses in key geographies. Drives awareness on impactful use of secondary data across the franchise • In priority disease areas, lead a cross-functional Real World Evidence team, consisting of representatives from cross-functional teams, embedded within a franchise and being a liaison to team members of the RWE team. With the clear objective to deliver and communicate scientifically valid and meaningful RWE to actively address the varying evidence requirements of partners e.g. Medical Societies, HCPs, Payers (HTA, Regional, Local), Regulators, Patient Groups • Utilize a decision matrix to determine with Medical Affairs / Patient Access / Safety / Product teams the most suitable source of RWD and RWE generation approach that meets prioritized evidence needs. Where secondary data is not available to generate fit-for-purpose evidence recommend the most appropriate prospective data collection study design and analysis that achieves the objectives. Provides input and supports to develop high quality functional and cross-functional plans • To implement and ensure uniform excellence standards across franchises for development and reporting of RWE studies. Member of the Integrated Scientific Review Committee (ISRC) with key oversight and advisory responsibility related to post-approval activities (including e.g. global/local phase IV, non-interventional studies, safety commitments). Chair Virtual Concept Review Forum a subcommittee of the ISRC, and guide CPOs on development of study concepts that are aligned with the franchise RWE strategy • Lead innovation pilots that can support to overcome key challenges in drug development using RWD or enable to provide meaningful RWE in support of regulatory decision making (e.g. label changes, new indications). Responsible for applying innovative RWE study design and statistical analysis to address the key research questions for the product and the Franchise • To work with regions and country colleagues on mapping of RWD sources, building research collaborations to increase the availability of fit-for-purpose RWD, licensing RWD that support local evidence generation in a robust and credible way Minimum requirements What you’ll bring to the role: • Advanced degree or equivalent education/degree in life science/healthcare required. • 6-8 year’s experience acquired at pharmaceutical companies, academia, or relevant consultancy companies • Deep understanding of Medical Affairs, Market Access/ HEOR, Safety or related disciplines to generate value evidence from retrospective and prospective studies. • Very strong understanding of drug development and commercial disciplines, proven ability to identify key evidence needs for Commercial, Market access, Medical, Safety, Regulatory stakeholders and lead a team towards building the required insights • Considerable experience in planning, creation, and analysis of real-world data, from both prospective and retrospective studies with a proven success record in this field • Experienced and with a strong knowledge of research methodology and statistical methods in the field of prospective clinical data analysis • Considerable experience in collaborating with quantitative scientists and analysts • Deep understanding of pharmaceutical value chain and its business processes • Ability to communicate effectively and motivate team alongside having a persuasive and credible presentation style at all levels of organization Desirable Requirements: • Previous work experiences in country organizations a strong plus • Knowledge of the IHD disease area WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking calculated risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarket AccessJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Berufslehre ab 7. August 2020 Chemie- und Pharmatechnologe/in EFZ

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Lehrstelle

Back to Previous Page Job ID281146BRPosition TitleBerufslehre ab 7. August 2020: Chemie- und Pharmatechnologe/in EFZApply to Job Job Description Frühere Berufsbezeichnung Chemikant / Chemikantin Chemie- und Pharmatechnologen sind die Produktionsspezialisten in der pharmazeutischen und chemischen Industrie. Sie bedienen computergesteuerte Anlagen, in denen hochwertige pharmazeutische, chemische und biologische Produkte hergestellt werden. Bei Novartis steuern und überwachen Chemie- und Pharmatechnologen chemische und biotechnologische Produktionsanlagen, in denen Schritt um Schritt Wirkstoffe für Medikamente hergestellt werden. Diese Aufgaben setzen voraus, dass Chemie- und Pharmatechnologen alle Anlagen in ihrem Arbeitsbereich genau kennen, ein gutes technisches Verständnis haben und über Grundkenntnisse in Technologie, Chemie und Physik verfügen. Minimum requirements Gute/r Sekundarschüler/in A Sekundarschule E oder Bezirksschule Technisches Verständnis, Verantwortungsbewusstsein, hohe Konzentrationsfähigkeit und gute Beobachtungsgabe, Zuverlässigkeit, gute körperliche KonstitutionDivisionNBSBusiness UnitHR NBSLocationSchweizSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaPraktikanten / Studenten bei Novartis PayrollJob TypeVollzeitEmployment TypeAusbildung Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Director Digital Business Strategy

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID286716BRPosition TitleDirector Digital Business StrategyApply to Job Job Description 2 million patient-years of data to unlock, 12 digital lighthouses scaling and industry leading partnerships! Welcome to Novartis Data & Digital! The last 24 months have seen tremendous momentum in bringing our data and digital transformation to bear! As we are moving from pilot to scale, we need to also evolve our own organization. We are hence hiring a Director Digital Business Strategy into the Digital Strategy and Operations team in Basel to drive key portfolio initiatives while also identifying and setting up longer-term business opportunities. We are on an exciting journey and if you enjoy exploring unchartered territory with highly dynamic team, then this is your opportunity! The team Digital Strategy and Program Operations reports directly to the CDO of Novartis and works with him in developing the overall digital strategy and operating model for Novartis as well as in driving select digital lighthouses and bold moves with cross-organizational and group strategic relevance. As the Director Digital Business Strategy in that team you would be responsible for developing and (co-)leading top priority digital projects mainly in the commercial space. These projects can focus on individual business units or span across the organization and will address key value levers in transforming our commercial model in especial but not limited to leveraging digital technologies for innovative commercialization approaches in the marketing space. You will also be responsible for working with the Head of the Digital Strategy and Program Operations in identifying longer-term, transformative business opportunities. Those priority efforts will be run jointly with the business or as exploratory efforts directly under the CDO. You will be expected to work with the senior leadership across our businesses and operating functions to drive and execute these efforts primarily in cross-organizational teams as well as with external partners as appropriate. This is a high visibility and demanding role, that offers the opportunity to shape the digital transformation at Novartis bringing together strategic thinking and operational execution for company-wide impact. You will be responsible but not limited to: As the Director Digital Business Strategy in that team your accountabilities will be: • Co-leads digital business projects mainly in the commercial space for the CEO and the Executive Committee and the CDO • Brings in deep expertise and acts as thought leader in the application of digital technologies and ways of working in go-to-market and commercialization approaches, including in digital marketing • Turns digital expertise into practice on the ground with the working teams • Largely independently manages cross-organizational teams and stakeholder groups • Proactively identifies trends and opportunities in the digital space that can shape the way Pharma operates in the future, incl. novel partnerships, go-to-market channels • Significantly contributes to the further development of the digital strategy • Takes on ad-hoc requests from CDO You will be expected to work with the senior leadership across our businesses and oper-ating functions to support the CDO in driving the digital transformation. Minimum requirements • Master or PhD in natural science or engineering MBA from a top business school preferred • High proficiency in English • 3-5 years of practical experience in Pharma and non-Pharma (e.g., consumer goods) in applying digital technologies with focus on go-to-market and marketing • 3+ years experience in strategy development with proven record on identifying and translating longer-term trends • Extensive experience and track record in project and program management of complex, cross-organizational projects • Track record of strong business impact and Capability to lead without formal authorityDivisionCORPORATEBusiness UnitDIGITAL OFFICELocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaBD&L & Strategic PlanningJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

USP Engineer - Plant 0 (80-100%)

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID282828BRPosition TitleUSP Engineer - Plant 0 (80-100%)Apply to Job Job Description 1 fully operational commercial-scale TRD technical Plant (Plant 0), that will enable the development & implementation of Novartis’s novel technology which is a paradigm shift in biologics manufacturing processes. The USP production engineer is required to plan and perform scientific experiments (or pilot plant processes) for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures in collaboration within a multifunctional project team coordinated by a Project leader. Responsibilities will include but are not limited to: • Meet quality, quantity and timelines in all assigned projects; Plan, organize, perform and document scientific experiments/plant activities and plan, perform and contribute to project related scientific/technical activities under minimal guidance and/or in collaboration with experienced team members (e.g. contribute to interpretation and report results); And seeks proactively for support and coaching from Project Leader, Scientific Expert or other team members during the whole process if necessary. • Provide efficient and robust processes for the manufacture and/or specialized facilities e.g. containment/sterile labs as an expert with adequate guidance; Utilize special tools/equipment and/or specialized facilities e.g., containment/sterile labs; Evaluate new lab equipment and contribute to maintenance of infrastructure/equipment; And keep record of and manage chemicals, intermediates, excipients and solvents within own area of responsibility. • Provide raw data documentation, evaluation and results interpretation; Propose and provide input for the design of next experiments; Optimize existing methods (lab or plant) and develop more efficient ones. Generate lab procedures, reports and/or instructions and/or SOP’s; and actively transfer procedures/instructions to pilot plant or production, including troubleshooting, process steering controls etc.; Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISEC & Novartis Guidelines. • Collaborate with other team members to facilitate deliveries of DS and/or DP; Communicate and address problems, perform safety and literature searches under moderate guidance from more experienced team member; Actively participate in project teams/meetings/networks and actively contributes to team goals; Ensure all own activities are aligned with overall drug development process. Strategic and scientific contribution to Networks, target achievements according to network charter and annual objectives Minimum requirements What you’ll bring to the role: • Technician with continuing education (EU) or BS or equivalent • Fluent in site-language. Adequate knowledge of English (oral and written). German is an asset. • Required experience: 3-5 years for BS/apprenticeship or 1-3 years for MS • Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment. • Skills and Knowledge: Good scientific or technical knowledge (e.g. synthetic, analytical, galenical). Proficient with laboratory and/or technical tools. Adequate knowledge of software and computer tools. Basic presentation skills and scientific/technical writing skills Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Trial Pricing Expert

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID269572BRPosition TitleTrial Pricing ExpertApply to Job Job Description 350! The number of active trials that GDO are running at present and each one comes to Early Pricing for comprehensive pricing solution prior to investment decision. As Trial Pricing Expert you lead stakeholders’ brief early in the process to estimate fully loaded trial costs, run benchmark analysis and modelling for realistic planning and study optimization and prepare pricing scenario for submission. Your responsibilities include, but are not limited to: • Deliver accurate and quality fully-loaded WP pricing estimations for assigned Project/WP in alignment with GPT / IMB portfolio review governance • Effectively translate clinical concepts into accurate and transparent fully-loaded WP pricing estimations (early and final), ensuring clinical and GPT operational strategic requirements are reflected with accuracy • Lead effective engagement and partnership with key GPT stakeholders to ensure alignment on pricing strategy in preparation of IMB submission • Integrate tollgate scenario modelling in final fully-loaded WP estimation for IC/ IMB submission • Identify early productivity savings and cost avoidance (consortium, synergies, footprint, and performance) • Develop comprehensive cost effective scenario options considering speed, price and operational execution for GPT/IMB consideration Minimum requirements What you’ll bring to the role: • • Bachelor degree in life science and/or bachelor degree in business with 7 – 10 years drug development or equivalent or, experience working in the pharmaceutical or CRO industry. Advance degree preferred • Proven ability to build strong, effective relationships with internal partners • Excellent understanding of the Clinical Development process and the management of clinical trials • Budget/forecasts management experience in Pharma research and development settings required • Fluent English (oral and written) WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Global Medical Affairs Director Ophthalmology

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID286839BRPosition TitleGlobal Medical Affairs Director OphthalmologyApply to Job Job Description 200 million patients worldwide are treated with Novartis ophthalmic products. Our Ophthalmology Franchise is re-imagining what’s possible by bringing life-altering treatments to patients with visual impairments and blindness. Medical Affairs Director role is providing key medical and scientific leadership to our brand medical teams and other brand related functions. Your Responsibilities: • Holistic approach to data generation aspects globally , focusing on generation and dissemination of medical information • Provide medical scientific input for the assigned Medical Affairs studies (Phase IIIB-IV, PMS, observational studies without regulatory impact) within program/brand, as a member of the Global Medical Affairs Team • Key activities related to planning, execution and reporting on Global Medical Affairs studies and ensure timely and on budget delivery. • Develop study-related documents, presentation material for study-related advisory boards, investigator meetings, protocol training meetings for Novartis local medical organizations • On-going review of clinical study data, final analysis and interpretation, in collaboration with the Brand Safety Leader, appropriate Global Clinical Team members and the Global Brand Team. • Build together with the Global Brand Medical Director/Portfolio GBMD a highly influential medical and scientifically based platform: a. Program/brand(s) publication plan and ensure execution in collaboration with assigned Medical Communication Leaders b. Support/ lead internal and external medical education and communication initiatives • Provide medical scientific input for the assigned program/brand(s) to: a. Develop integrated Product Strategy, MA strategy and related MA plan b. Develop Clinical Development Plan c. Guide and develop local MA clinical programs and provide support in execution d. Value dossiers and participation at payer advisory boards e. Lead Medical Affairs Study Team to provide guidance to CPOs (Country Pharma Organization) related to their MA study program; review, approve and follow up on local MA studies • Support GBMD/portfolio GBMD in ensuring compliance of promotional and non-promotional global material and all Medical Affairs activities. • Support or deputize GBMD/Portfolio GBMD in providing input into brand safety related activities or in a Global Clinical Team, Global Brand Team, Clinical Scientific Unit and internal decision boards as the Medical Affairs spokesperson. Minimum requirements What you’ll bring to the role: • MD or PhD with unique knowledge for successful clinical program development and execution, with ≥ 6 years of clinical research experience required. Or MD with specialty with board certification • Ability to run studies and write a protocol with advanced medical/scientific writing and communication skills • Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area. • Proven ability to work both independently or in a cross -functional team setting, including a matrix environment. • Demonstrated ability to establish strong scientific partnership with key investigators in assigned TA. • Medical and/or scientific expertise within Ophthalmology is an advantage • Fluent English (oral and written) Why consider Novartis? 817 million. That’s how many lives our products touched in 2018. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.DivisionPHARMABusiness UnitGLOBAL MEDICAL AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Region Europe Brand Director - Gene Therapy (80-100% )

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID278730BRPosition TitleRegion Europe Brand Director – Gene Therapy (80-100%*)Apply to Job Job Description 20! The number of years to develop the product; a transformational gene therapy for children and adults impacted by an ultra-rare retinal disease that causes the ongoing deterioration of vision cells and leads to complete blindness. Join our team on an incredible journey to expand the reach of the first ever ocular gene therapy. We target a disease that lacks effective therapies and affects relatively small numbers of patients, many of whom are children. Reporting to the Head of Region Europe for the product, the Region Europe Brand Director (REBD) - with focus on Gene Testing - will shape the regional strategy and lead execution of commercial strategies to accelerate identification of patients who may be appropriate for treatment. Your responsibilities will include: • Effectively partner with relevant Country Commercial Leads in Country Pharma Organisations (CPOs) to assist them and ensure fit-for-purpose diagnostic/ genetic testing strategies • Understand the various diagnostic patient journeys in the CPOs and in collaboration with internal and external stakeholders, develop programs/activities to improve the patient journey • Drive genotyping diagnostic efforts through regional disease awareness and education initiatives • Identify and develop Genetic Testing KOLs. Deliver and implement speaker disease and diagnostic educational programs • Lead the partnership efforts with Genetic Labs performing high quality gene analysis that offer the appropriate IRD panels with clear interpretation of results • Lead the effort to expand genetic testing and streamline efforts across Region Europe Minimum requirements What you’ll bring to the role: • Must have experience with Hereditary Gene Testing or Companion Diagnostics • Extensive (> 10 years) of pharmaceutical, biotech or medical commercial experience • Passion and genuine commitment to supporting rare disease communities • Strong organizational and project management skills, demonstrated ability to successfully drive a project to completion • Strong leader to drive change and influence others, without direct report responsibility, across functions (medical, sales, patient access) and countries Desirable requirements: • Successful launch experience in a biotech, specialty or rare disease role • High level presentation and interpersonal skills; able to communicate and present ideas to stakeholders in a way that produces understanding and impact that builds effective partnerships WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionPHARMABusiness UnitREGION EUROPE GENMEDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Chief Scientific Officer, Switzerland

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID287496BRPosition TitleChief Scientific Officer, SwitzerlandApply to Job Job Description 8! The number of new drug launches planned over the next 2 years. Your medical team will help understand what these medicines do, why they matter for the patients, and how Novartis is striving to reimagine medicine through the leading industry pipeline of medical innovations. As our Chief Scientific Officer (CSO) you will be the top medical scientist in the country, responsible for clinical research, overall medical strategy, medical education and external engagement with the medical community for Novartis Pharma. As a core member of the Business Unit and Regional Medical Leadership Teams, you will be accountable for the creation of the functional Medical strategy for the country and ensure its execution, by leading all clinical and medical aspects of in-country activities and all associated resourcing and performance aspects. In partnership with country Regulatory Affairs, you will develop and manage long-term relationships with local Regulatory agencies and relevant medical societies. In close partnership with other country stakeholders, you will coordinate and ensure accelerated access to Novartis medicines. Your responsibilities will include: • Shape and drive long-term medical strategy for the country regarding all scientific, medical and clinical aspects in line with Global, Regional and Country/Cluster needs. Ensure optimal pre-launch preparation and market readiness at least 2 years prior to launch • Medical Excellence: Lead the local Medical Affairs teams, develop overall direction and priorities and ensure execution via performance objectives and metrics (tracking of all medical activities etc.). Ensure the effective deployment, training and work execution of both the field medical associates (MSL) and Medical Advisors • Ensure compliance adherence in all medical activities and quality in the execution of all medical-related business practices on a country level; provide medical expertise to other functions • In close collaboration with GDO, ensure strategic and effective allocation and execution of clinical trials within the country • Ensure close cross-functional collaboration with key internal stakeholders including Patient Access, GDO/Regulatory Affairs and Patient Safety to support patient access to Novartis medicines; improve patient journey in close collaboration with the Disease Management Lead; ensure cross-functional collaboration with Patient Access and Commercial, in compliance with Novartis policies • Plan, execute and interact with key external stakeholders and represent Novartis at key external scientific, clinical and medical events to support evidence-based research in the relevant Therapeutic/Disease areas • Scout and identify innovative ideas, medical-business collaboration with external stakeholders in the medical and related area to drive business acceleration, set up new projects and/or events [#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • Medical Doctor (not required, but a big plus) or PhD or PharmD, strong scientific competence • Pharma market experience (e.g. previous CSO or TA Head or Global/Regional Medical role); knowledge of Switzerland market and KOLs is a plus: Experience of pre-launch and launch in Pharmaceuticals, experience from (leading) field medical (=customer facing) roles, experience of managing clinical development processes • Strategic mindset, strong Business Acumen, out of the box thinking, change agile • Leadership presence: Strong influencing & presentation skills, proven successful people management experience, ability to work in a highly matrixed organization • English fluency. German knowledge not required but a big plus, French is a further plus WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitREGION EUROPE GENMEDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma Schweiz AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Real World Evidence Director, Cardio (80-100 )

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID287658BRPosition TitleReal World Evidence Director, Cardio (80-100*)Apply to Job Job Description Decades of untapped unmet needs in the Cardio-Renal-Metabolic (CRM) space are waiting for your footprint and guidance! As part of the long-term CRM strategic and operational growth plan, this is an ideal opportunity to bring new innovative products to those in need. We seek to become the leading innovators in the CRM space by developing a transformative Precision Medicine specialty portfolio for areas of high-unmet medical need. Our new Real World Evidence Director role based in Novartis’ Headquarter, in collaboration with a very diverse team, will provide, assess and bring life-saving drugs to patients globally! Your responsibilities will include: • To ensure a broad understanding of the value of RWE to the product value demonstration both globally and locally. Lead and ensure innovative, best-in-class evidence planning and creation, to maximize value of key development projects, products, and businesses in key geographies. Drives awareness on impactful use of secondary data across the franchise • In priority disease areas defined by Franchise Medical and Patient Access heads, and focused on gaps, lead a cross-functional Real World Evidence team, embedded within a franchise and being a liaison to team members of the RWE team. With the clear objective to deliver and communicate scientifically valid and relevant RWE to proactively address the varying evidence requirements of stakeholders e.g. Medical Societies, HCPs, Payers (HTA, Regional, Local), Regulators, Patient Groups • Utilize a decision matrix to determine with Medical Affairs / Patient Access / Safety / Product teams the most suitable source of RWD and RWE generation approach that meets prioritized evidence needs. Where secondary data is not available to generate fit-for-purpose evidence recommend the most appropriate prospective data collection study design and analysis that achieves the objectives • To implement and ensure uniform excellence standards across franchises for development and reporting of RWE studies. Member of the Integrated Scientific Review Committee (ISRC) with key oversight and advisory responsibility related to post-approval activities (including e.g. global/local phase IV, non-interventional studies, and safety commitments). Chair Virtual Concept Review Forum (VCRF), a subcommittee of the ISRC, and guide country organizations on development of study concepts that are aligned with the franchise RWE strategy • Lead innovation pilots that can support to overcome key challenges in drug development using RWD or enable to provide meaningful RWE in support of regulatory decision making (e.g. label changes, new indications). Responsible for applying innovative RWE study design and statistical analysis to address the key research questions for the product and the Franchise Minimum requirements What you’ll bring to the role: • Advanced degree or equivalent education/degree in life science/healthcare required. MBA or equivalent preferred • 8+ years of relevant pharmaceutical industry experience, academia, healthcare provider, payer, HTA, or relevant consultancy companies • Deep understanding of Medical Affairs, Market Access/ HEOR, Safety or related disciplines to generate value evidence from retrospective and prospective studies. Very strong understanding of drug development and commercial disciplines, proven ability to identify key evidence needs for Commercial, Market access, Medical, Safety, Regulatory stakeholders and lead a team towards building the required insights • Considerable experience in planning, creation, and analysis of real-world data, from both prospective and retrospective studies with a proven success record in this field Aim for five bullet points • Considerable experience in collaborating with quantitative scientists and analysts Desirable requirements: • Cardio, Renal, Metabolic therapeutic area experience • In country experience *Some restrictions on flexible working options may apply and will be discussed during interview if applicableDivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarket AccessJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Global Marketing Director, CRM (80-100% )

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID282836BRPosition TitleGlobal Marketing Director, CRM (80-100%*)Apply to Job Job Description 26 million! That’s how many people are affected by Heart Failure worldwide. More people die from heart failure than from some advanced cancers, including breast and bowel cancer, and it is the biggest single cause of hospital admissions in adults aged over 65 in the western world. As a leader in heart failure, we are now looking for a Global Marketing Director to join our team in our efforts to reimagine outcomes for people living with heart failure. Specifically, we are looking for a creative marketer, with experience working with global brand building, in both large country and global organizations, with both consumer goods and pharmaceuticals. As a Global Marketing Director, you will provide leadership to the global brand team on the development and execution of the marketing strategy for our leading heart failure therapy. You will work in close collaboration with other global functions and countries to improve brand value across target customer groups. Your responsibilities will include: • Lead the development of brand messaging and communication strategies, across customer groups • Own the development and launch of new initiatives and campaigns including selection and management of multiple agency partners • Provide leadership to design and delivery of marketing mix, balancing value with brand KPIs • Drive new insights through integration of data from multiple sources, including market research studies, primary/secondary data and competitive intelligence • Model strong collaboration and partnership with key partners to ensure optimal effectiveness and delivery of brand marketing strategy and deliverables Minimum requirements What you’ll bring to the role: • A minimum of 8 years of operational and strategic Marketing experience both in and above countries with extensive focus on product/brand management and in customer facing/sales roles • University degree in Science and/or degree in Business Marketing or Clinical Research • Effective people leader with proven experiences and track records of people leadership • Experienced in leading interactions with very senior stakeholder (internally & externally) independently • Track record of building strong and disruptive brand strategic plans Desirable requirements: • US experience, or experience in other larger markets • Launch experience with new products or major line extensions • Experience in heart failure category and/or adjacent cardiovascular therapeutic areas • Languages in addition to English WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Global Medical Affairs Associate Director, Field Medical Excellence

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID286315BRPosition TitleGlobal Medical Affairs Associate Director, Field Medical ExcellenceApply to Job Job Description In your role, you will be responsible for the implementation of our Global Oncology MSL Excellence Program, Medical Science Liaison (MSL) communication plan development and oversight of MSL metrics and analytics. Your responsibilities will include: • Lead implementation of the overall communication platform for the MSL Leadership Team and MSLs worldwide in collaboration with Scientific Engagement and Communication (SEC) leadership. • Partner with MSL Insights Teams across Onocology Business Unit portfolio to lead insight monitoring, communications and monitoring of Action Plans. • Develop change management plan for implementation of Global MSL KPIs, metrics and analytics. • Develop communication plan for the Global MSL Onboarding Program and Scientific Engagement Approach; and lead assessment of impact of the programs. • Oversee implementation of the MSL Development/Talent program (eg, MSL Mentor Network, MSL 2x, Global workstreams, etc) and conduct benchmarking to identify solutions to enhance MSL career development and retention. • Generate communication plan and implement training for MSL digital tools through partnership with Multichannel Engagement (MCE), PLS and Digital Team Leads. • Lead congress medical booth process and partner with NBS/PLS for medical booth staffing, communications, logistics (iPads) and budget at key international congresses. Minimum requirements What you’ll bring to the role: • Advanced degree (e.g MD, PharmD, PhD) or equivalent education/degree in life science/healthcare is preferred • Excellent interpersonal, written and oral communication skills • 7+ years’ experience in pharmaceutical or healthcare related industry • Prior experience in the MSL function • Understanding of the pharmaceutical business, including drug development process and legal/compliance global environment • Excellent working knowledge of Medical Affairs activities including Medical Information, Medical Education and Scientific Exchange Excellent organizational skills and ability to manage complex projects • Experience collaborating cross-functionally and across countries/regions preferred • Oncology therapeutic knowledge preferred WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Senior Specialist BioSample Compliance (80-100 )

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID286522BRPosition TitleSenior Specialist BioSample Compliance (80-100*)Apply to Job Job Description 6500! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. The Scientific Operations department at Novartis Institutes for BioMedical Research (NIBR) is looking for a BioSample Compliance associate who will be supporting the BioSample Compliance group in ensuring operationally the compliant use of human biosamples with respect to internal policies, guidelines, and applicable local and national laws and regulations at our research sites. You provide technical guidance and training to researchers and internal/external partners and by monitoring compliance in their day-to-day application of defined local guidelines, you ensure that research activities at NIBR are in alignment with our mission. Minimum requirements What you’ll bring to the role: • Minimum BSc/MSc in biological sciences • German, English • Sound knowledge of Human BioSample compliance documentation review, analysis, elaboration and submission • Scientific and research background, knowledge of the Swiss Human Research Act (HRA) and Embryonic Stem Cell Act (StRA) would be a plus • Thorough experience in understanding legal documents Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNIBRBusiness UnitCFOLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Service Delivery Manager Commercial Data

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID273777BRPosition TitleService Delivery Manager Commercial DataApply to Job Job Description This critical role will lead Novartis Commercial Insights strategy, roadmap definition, use of data as key strategic asset - in collaboration with Business stakeholders (e.g. Product Owners) - to maximize value generation for Sales and Marketing. The SDM Commercial Data and 360 Insight represents IT to the business ensuring that expectations for IT services are met. Candidate is able to work independently, with pragmatism and masters the Data/Analytics Commercial strategic initiatives as well as the Agile methodology. Key success will be defined through intimate understanding of the Sales and Marketing and Business processes and key objectives, customer journeys and value realization maximization. The scope covers both Oncology and Pharma Divisions. Drive transformation into new ways of working in order to deliver harmonized enterprise data models and insights products. You will be responsible but not limited to: • Collaborate with Business and IT Leaders to drive - Market and Customer insight strategy and roadmaps definition • Translation of these strategies into Global Commercial Strategic initiatives plan (ICON, DROID v3, DICE v3, CONNECT, ACT Data AA, MDM Deep Blue) • commercial processes, solutions / products functionalities gaps identification - continuous end users experience optimization • Define uses cases for these users - planning and identification of appropriate data sources, data models, best in class Metrics/KPIs and Visual solutions / technology to close these gaps • Value generation optimization (qualitative and quantitative benefits planning and measurements) - users adoption and satisfaction optimization (including planning and measurement) - internal solution / product promotion and training (e.g. product catalogue) • Liaise with the service development and deployment teams (e.g. Analytics COE, Project Execution) to ensure successful execution of Global Commercial Strategic initiatives (ICON, DROID v3, DICE v3, CONNECT, ACT Data AA, MDM Deep Blue) • Develop project / use cases estimates, feasibility assessments, business cases - manage budget and Third Parties with efficiency, accuracy and transparency - drive internal IT approval processes (e.g. DRC, ITIC, …) • Ensure efficient and compliant product releases mgmt (Agile) / consistent traceability between user requirements, functional specifications and testing (waterfall) • Act as internal “Agile” champion in data and insights space / Novartis IT and Business organization and help promoting SCRUM values (personal commitment, courage, focus, openness, respect) • Keep abreast with internal IT systems and documentation requirements, standards (including quality management and IT security), industry best practices Minimum requirements • Bachelor Degree in Computer Science, Engineering, Information Technology, or Business • Admin Higher degree in any of the above disciplines is preferred • Business fluent in English (written and spoken) • +15 years of business and IT Mgmt experience at Global/Regional/Local levels +10 years of Global Program Mgmt and Data Mgmt and Business Intelligence experience. • Advanced Analytics, Machine Learning experienced preferred. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionNBSBusiness UnitIT NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Novartis Digital (data42) - Are YOU curious?

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID284677BRPosition TitleNovartis Digital (data42) - Are YOU curious?Apply to JobSourcing Statement You are applying to be part of the Novartis Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV. Job Description Are YOU ready to unlock the full potential of 2 million patient-years of R&D data to improve how we develop medicines for patients? Our Organization: 2 million patient-years of data! data42 is Novartis’ groundbreaking program to utilize data in one of the largest and most diverse datasets in the pharma industry, with the ultimate goal to change and improve how we develop medicines. At Novartis, we believe that Artificial Intelligence, combined with the wealth of our data and internal scientific expertise, will transform life sciences. data42 is a holistic R&D connected data & analytics ecosystem built for Novartis Scientists to accelerate the delivery of new medicines to patients. data42 will drive the adoption of machine learning and artificial intelligence in the daily work of scientists, apply advanced analytics to derive insights that contribute to grow our understanding of disease and medicines, enhance R&D decision-making and ultimately reimagine drug discovery and development. Impact Of This Position: Our culture is at the center. We work through agile, unbossed teams who feel passionately about driving value. We are building a platform and data-lake that ingests and unifies all Novartis R&D data and enables our data scientists and data explorers to quickly access, analyze, and derive previously impossible insights from our data. We are crafting reusable products that bring to bear the platform, data, and assets to drive real business value and help our researchers answer the questions that will bend the curve of life... These are our goals, ultimately! To ensure this dream becomes a reality and to accelerate data-driven insights to facilitate a breakthrough in innovative medicines for patient’s needs, we will need your support. We are seeking innovative, independent and dynamic team members, preferably with experience gained in the pharmaceutical industry, to join a transformative movement within Novartis to shape the way we develop medicines. Researchers, scientists, data engineers, development & technology leads, and agile scrum masters & coaches; we need you. EEO Statement The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Minimum requirements Desired Requirements: You will actively help reimaging medicine with the goal to discover and develop novel therapeutic treatment options. If You Are: • Obsessed about impact: -We enable and perform analysis that makes a difference. You’re motivated by our vision and excited by the contribution you can make personally in delivering better medicines to more patients, faster. • Collaborative and creative: - You will work in small cross-functional teams, empowered to discover, own, and solve problems creatively. You can communicate your ideas and results effectively with colleagues and partners outside of your field. • Intensely curious: - You dig beneath the surface of a problem, interrogate the question and synthesize clear hypotheses that can be engineered and tested. • Always seeking better: -You capture insights and use data feedback loops to iterate and re-invent, to better address the scientific questions our users wish to answer. • Ego-free: - Power brokers are not of interest to Us. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous, and collaborative people like you are brought together in an inspiring environment, where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Full Stack Machine Learning Engineer

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID277333BRPosition TitleFull Stack Machine Learning EngineerApply to Job Job Description 130+ bots live and many in the pipeline! An innovative multidisciplinary IT team in Novartis, you will be part of the integral talent in collaborative innovative and agile teams that experiment, rapidly incubate and establish to scale digital platforms that deliver value to Novartis in areas like Process Automation, Cognitive Computing (AI, ML), Natural Language Processing, etc. Job purpose: • Design and Build automation solutions leveraging Machine Learning patterns. • Elaborate Machine Learning design patterns which adequately responds to a given business/technical automation problem – and continually evolve them for higher efficacy. • Lead the development of identified end to end solutions. Accountable to define machine learning solution: • Understand technology and infra constraints (eg: models, efficacy, data etc.) to conceptualize solutions within tight constraints of time & technology. • Elaborate and describe the solution design holistically. • Develop, build, configure and unit test solutions • Perform all work to agreed time, cost and quality constraints • Ensure that developed solutions are peer reviewed and formally documented • Validate solution design of the machine learning automation solutions regarding their adequacy and adherence to requirements and standards throughout the solution lifecycle. • Track performance of the model/product once live and iterate the design of the machine learning models to achieve needed efficacy. • Work with Delivery teams/BEF/Business SMEs to give inputs regarding the right end-to-end operating model for ML-solutions. • Own support for product technology related issues to project and operations teams • Define how the different solution components will need to interact and enable their implementation by the delivery teams. • Accountable for design, build and maintenance of reusable assets and components on technology Minimum requirements • Masters in Computer Science/Machine Learning/Statistics or equivalent areas • Fluent in English, other languages beneficial • Hands-on, passionate technologist with a ‘maker mindset’. • At least 6-8 years total experience in IT in which at least 3-4 years is with designing and implementing AI/ML/NLP solutions • Experience with using pre-configured ML services out of Azure/AWS to build out solutions. • Experience building and deploying ground up ML models with Linear/Logistic Regression, Decision trees, Naive Bayes, Random Forest etc. • Proficiency with one or more of the leading deep learning software packages: TensorFlow, Keras, PyTorch, or MXNet • Global Mindset and communication skills; stakeholder influencing skills • Experience and capability to work with different internal and external roles in a matrix organizational setup WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionNBSBusiness UnitIT NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Principal Scientist in Particles Lab (Biologics) (80-100%)

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID284337BRPosition TitlePrincipal Scientist in Particles Lab (Biologics) (80-100%)Apply to Job Job Description 200! The approximate number of Clinical Development projects currently in the Novartis pipeline. Many of these projects, which include new biological entities, are for medicines that could significantly advance treatment standards for patients worldwide. Within physical-chemical analytics (PCA) in late phase biologics development, all Novartis new biological entities (NBEs) are supported from proof-of-concept in human to commercialization and up to life-cycle management activities. PCA, which is an integral part of the Analytical Development and Characterization unit within Global Biopharmaceutical Product and Process Development, applies a wide range of analytical techniques to characterize the biopharmaceutical products. The successful applicant will be part of the Special Analytics group working in a highly collaborative and scientific environment, and will work in close interaction with stakeholders covering all steps in NBE development. Responsibilities will include but are not limited to: • Determination of visible/sub-visible particles in therapeutic protein formulations using state-of-the-art technologies. • Interpretation of results to support formulation and process development, root cause investigation, comparability assessment, etc. • Maintenance and qualification of lab equipment, • Development of methods and implementation of new technologies. Minimum requirements What you’ll bring to the role: • University degree in Biochemistry, analytical chemistry or related field with minimum of 2 years of directly related scientific experience for PhD, 5 years for Master of Science or 10 years for Bachelor of Science. • Hands-on experience in particle analysis as well as excellent theoretical and practical knowledge of state-of-the-art particles analysis technologies (e.g. Flow imaging, Light Obscuration, Static and Dynamic Light Scattering, Resonant Mass Measurement • Broad theoretical and scientific knowledge in pharmaceutical development of biologics molecules. • Ability to interpret and present scientific information critically and objectively. Strong scientific project management skills. • Strong inter-personal skills ensuring close collaboration with multiple teams on a global level, effective communication with internal and external partners, and the ability to work in international teams. • Advanced scientific/technical writing skills, thorough understanding of development activities and processes as well as good understanding of regulatory expectations. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Global Category Procurement Head - Clinical Development (80-100% )

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID285188BRPosition TitleGlobal Category Procurement Head – Clinical Development (80-100%*)Apply to Job Job Description Why consider Procurement? At the front line of this critical commercial challenge is the R&D Procurement Team. When you join the R&D Procurement Team, you join a global organization impacting over 80,000 patients per year, supporting 90+ new molecular entity projects, 500+ clinical trials with ~100 new trials initiated per year, 15 development centers globally, supporting 70+ countries, while influencing over $10Bn in total R&D spend. Turning ideation into reality, the R&D Procurement Team helps shape the R&D strategy leading all commercial engagement, negotiations and third-party management to drive our world-class organization to lead the industry in R&D. As our Global Category Procurement Head, Clinical development, you will lead all strategic procurement aspects within the category of Clinical Development, on a global level and in collaboration with Global Drug Development (GDD). In alignment with Global Development Operations (GDO) & External Development Operations (EDO) and other functional stakeholders within GDD, you will develop procurement category strategies and strategic approaches related to the management of 3rd party spend in the area of clinical development. You will build up, lead and run a global team of Category Leads, sourcing managers and buyers through design, implementation and execution of business-aligned procurement strategies for relevant subcategories of spend. Further, you will be the primary procurement business partner for GDO in the area of Clinical Development, ensuring budget-alignment, strategy and productivity achievement, including design and delivery of margin expansion initiatives across Novartis. You will collaboratively drive all necessary internal alignments to ensure an effective procurement processes end to end and provide high value external solutions to the business stakeholders. Your responsibilities will include: • Drive / Implement category strategic goals from overall Procurement strategy, ecosystem management • Deriving game-changing strategies by defining clear category objectives, working with analytical data, business partners and market expertise. Aligning strategies to measurable target and clearly conveying them to the organization • Executing the Novartis Strategy for the relevant functional area, with profound commercial & technical skills as well as solid procurement knowledge • Driving Procurement strategy based on insights into procurement leading practices and experience into category strategy development and execution. Linking Procurement strategy to Novartis and functional business area and conveying it clearly to business stakeholders, procurement associates and relevant 3rd parties • Mapping the value chain, analyzing it and deriving potential scenarios. Includes the understanding and application of total cost of ownership, and should cost modelling analysis • Compliance & risk management: supporting reports to determine appropriate compliance level. Monitoring end-to-end compliance (budget, payment, vendor PO, contract invoice, buying channel, etc.) and deriving corrective actions to improve compliance • Applying risk management processes including identifying and evaluating risks, and defining and executing a risk mitigation plan • Projecting the dynamics and impacts (e.g., mergers and acquisitions). Extracting, cleansing and consolidating information to fact-based insights for further usage e.g. in category strategies • Participating in and / or leading financial discussions. Applying financial knowledge to participate actively, e.g. in budgeting process, including tax aspects in sourcing strategies and structuring sophisticated deals with ecosystem partners • Support definition and implementation of Procurement tools and processes • Managing data analysis and reporting, e.g. analyzing spend, demand, supply markets and competitors. Extracting, cleansing and consolidating information to fact-based insights for further usage e.g. in category strategies • Demand management - Responsible to ensure the right balance between business needs and Novartis’ strategy - Accountable to work with stakeholders to identify the most cost-effective ways to deliver business objectives • Strategic Sourcing and supplier relationships management Minimum requirements What you’ll bring to the role • University/Advanced level degree needed • Master’s Degree/other advanced degree in the Business or Clinical based disciplines is preferred • Excellent Spoken and Written English • Other foreign languages as required • >10 years of relevant Clinical Development business experience, preferably developed on the CRO side • At least 10 years of experience in CRO Management and associated clinical services • At least 5 years of experience in category management, supplier management, or related area, with a focus in Clinical Development • Strong Clinical knowledge to be credible with the Novartis Global Drug Development community • Demonstrable leadership experience WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNBSBusiness UnitPROCUREMENT NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaProcurementJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Biopharmaceutics Science Lead (80-100% )

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID277694BRPosition TitleBiopharmaceutics Science Lead (80-100%*)Apply to Job Job Description ~400! This is the number of associates in Global Pharmaceutical Development, across 4 countries, working tirelessly on innovative and patient centric pharmaceutical dosage forms for oral, parenteral, topical and inhaled administration routes. As part of this group, the biopharmaceutics community at Novartis is waiting for you to take on the scientific leadership in Biopharmaceutics and shaping biopharmaceutics based drug product development. By bridging the pharmaceutical science to the clinical performance you will drive the transformation of our molecules into medicines that improve and extend patient’s lives. The position is based in the Novartis Headquarter in Basel, Switzerland, within the Technical Research and Development Organization (TRD) of Global Drug Development (GDD). As Biopharmaceutics Science Lead, you will provide expert scientific leadership in Biopharmaceutics, ensuring that the Global Pharmaceutical Development (GPHAD) unit has the capabilities to perform at world-class level in biopharmaceutics based drug product development. Your responsibilities include but are not limited to: • Drive excellence in our research and development projects through technical oversight of our portfolio. Provide expert scientific leadership in Biopharmaceutics. Closely working with Drug Product development project teams to develop a full understanding of the drug substances and dosage form (formulation and process) factors affecting in-vivo performance of our medicine along with the relevant product control strategies across all route of administrations. • Drive and influence use of biopharmaceutics methods and tools (Modeling and simulation and biorelevant dissolution testing) in drug product development and define best practices. • Proactively identifying potential scientific, technological gaps, proposing creative solutions and ensuring appropriate communication within and across units. • Author and review biopharmaceutics reports (e.g. absorption modeling, or biorelevant dissolution), including relevant CMC documentation for clinical and marketing applications. Support project team in defining the regulatory biopharmaceutics strategy and HA interactions. • Drive and lead initiatives to advance science, technology and innovation within the area of biopharmaceutics aiming to obtain better predictive biopharmaceutics methods or improved drug delivery, includes identifying and participating to external consortium or initiative. Minimum requirements What you'll bring to the role: • Advanced degree in scientific or relevant discipline (PhD or equivalent) • Recognized scientific/technical expertise in biopharmaceutics area and broader scientific and strategic background • Broad and in-depth understanding of drug development processes and the contribution of pharmaceutical development from lead optimization to launch • Excellent knowledge of biopharmaceutics tools for the characterization of API and dosage form and modelling and simulation software in the biopharmaceutics area. • Proven leadership experience in managing projects ideally in a global matrix environment • Fluent in English (oral & written). WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interviewDivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Intern Biostatistics MSc

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Praktikumsstelle

Back to Previous Page Job ID284874BRPosition TitleIntern Biostatistics MScApply to Job Job Description 700 ! The number of days we can get therapies faster to patients applying technology innovation. The internship will focus on the development and/or application of statistical methods in clinical research and development. Mathematical, statistical, graphical or programming techniques will be used for data analysis, simulation and display. This internship will provide motivated students with an exposure to pharmaceutical industry and with the opportunity to work in an exciting, multi-disciplinary and multi-cultural environment with senior-level biostatisticians. The intern will also be able to participate in a variety of educational opportunities within the biostatistics function of the Integrated Quantitative Sciences (IQS) department. The internship is expected to last approximately 3 months, or up to 6 months. Minimum requirements The candidate should be familiar with common statistical methodology and be interested in its application in drug development. Good written and oral communication skills in English are required. Programming skills in a statistical programming language such as SAS or R are expected. The candidate should hold should hold a Bachelor’s Degree equivalent in Mathematics, Statistics, or related subjects, and be enrolled in a MSc or just finished the MSc. Language: English Duration: 3-6 months Why consider Novartis ? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternship Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Global Marketing Director New Products, Hepatology (80-100%)

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID285392BRPosition TitleGlobal Marketing Director New Products, Hepatology (80-100%)Apply to Job Job Description With over 15 innovative development projects that could transform care for more than 300M patients worldwide, the IHD New Products Team is working to reimagine the medicines of the future. We work closely with our Research, Development and Commercial colleagues to maximize the impact of our portfolio on patients and healthcare systems. Your responsibilities will include: • Provide commercial input to guide the development program and life cycle plans to optimize commercial potential • Liaise with Novartis Institutes for BioMedical Research (NIBR) to support project milestone transitions decisions, and maximize the strategic fit of drug research activities and liaise with key country organizations to ensure appropriate country & regional input to program strategy • The NPD is also the lead commercial support for external opportunities focusing on Hepatology. This requires liaising with BD&L to identify, screen and assess potential in-licensing opportunities, and provide disease area expertise and commercial input • The NPD is a key contributor to the creation of market-driven disease area strategies, creating and refining target product profiles (TPP) with clearly differentiated competitive advantage and Value Propositions (in GPT, NIBR programs and BD&L • Develop, implement and lead market research plans for programs for which you are responsible and ensure that key insights are incorporated into GPT clinical development and market access strategies • Use in-depth disease area and market knowledge to influence development colleagues, providing strategic direction to clinical trial design • Drive early brand value and differentiation through formulation development and packaging, including new technologies, brand vision, strategy, positioning and strategic imperatives to achieve financial objectives, and aligning company resources Minimum requirements What you’ll bring to the role: • PhD/MD/MBA or relevant business consulting experience • Commercial mindset & with experience in Commercial assessment of BD&L / M&A opportunities • Minimum 5–7 years professional experience in Pharma industry • Strong influencing skills, both internally and externally. Proven ability to work successfully within a matrix organization with ability to lead cross-functional teams without authority • Strong external networks in appropriate disease area Desirable Requirements: • Experience in early product commercialization or pricing and market access also desirable • In-depth knowledge in appropriate Immunology, Hepatology & Dermatology disease area desirable • Experience in multiple geographies and or sales experience desirable WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Global Program Associate Director (GPAD)

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID284225BRPosition TitleGlobal Program Associate Director (GPAD)Apply to Job Job Description 200+ The number of R&D projects underway which are supported by the Novartis Global Program Teams, all facilitated by associates in Global Program Management. The Global Program Associate Director role is critical to: • Providing program/project management expertise and operational support for highly complex global drug development programs or brands. As a member of the Global Program Team (GPT) the GPAD maintains accurate plans, documentation, and resource forecasts. • Supporting the Global Program Executive Director (GPED) to ensure smooth day-to-day operation of the GPT, resolving program issues, and facilitating alignment across sub-teams and line functions. Your responsibilities may include but are not limited to: • Contributing to the cross-functional strategy and program scenario generation to enable efficient GPT discussions • Identifying and managing program development risks and issues • Enabling an enterprise view when planning resources and budget • Generating and maintaining a high-quality and accurate project plan and forecast in the enterprise planning system (e.g. Horizon) • Monitoring and tracking development activities to forecast, timelines and at high quality • Facilitating GPT dynamics, performance and communication The GPAD is a project management professional with expert planning and tracking skills. Minimum requirements What you’ll bring to the role: • Masters or Doctorate in life sciences (or MBA with Bachelor’s degree or equivalent experience in life science). • Fluent English (oral and written). • 5+ years in the pharmaceutical industry with 5+ years (or equivalent) with multi-/cross functional team experience • Strong program/ project management skills and experience in drug development required • Previous track record of success working with large scale and complex international and multidisciplinary drug development teams • An intermediate knowledge of the drug development process • Expert planning and tracking skills, ability to use proper program management tools • Well organized, focused on results, capable of managing multiple projects, excellent time management skills with respect to priorities and self-management • Strong interpersonal and communication skills (written and verbal) for bridging across diverse, cross functional, multi-national, geographically dispersed teams WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitPORTFOLIO STRATEGY & MGMT GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Senior Data scientist

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID272904BRPosition TitleSenior Data scientistApply to Job Job Description 30 petabytes of 30 varieties of data forms across the value chain is waiting for data scientists to unlock the potential. Open source technologies, advanced deep learning algorithms, time for innovation is what we offer to folks who can apply to a problem solving hungry business to bend and improve patient life. Data Scientist is responsible for the capabilities needed to operate a scientific practice using advanced techniques to understand data and produce insights that are of value to Novartis. The role encompasses the full life cycle- from design, implementation and rollout of the solutions. The mission is to solve scientific, operational and technical challenges. You will be responsible but not limited to: • Collaborate in multi-functional teams to evaluate business activities, and then develop innovative and effective approaches to tackle team’s analytics problems and communicate results and methodologies. • Ability to initiate and drive projects from conception to completion with minimal guidance. • Innovates and recommends advanced predictive analytics, computational science, Natural Language Processing (NLP), machine learning and deep learning techniques to answer research questions and synthesize insights that achieve business objectives. • Establishes scalable, efficient, automated solutions for large scale data analyses, model development, model validation and model implementation. • Works to translate prototypes into new products, services, and features and provide guidelines for large-scale implementation. • Ability to build and fine tune algorithms that scale up from small-scale proof-of-concept stage to full production systems • Build knowledge artifacts of real business problems that were solved with advanced analytics techniques which can be published in journals. Minimum requirements • University degree in Statistics, Operational Research, Computer Science or in a highly quantitative field. • Business fluent in English (written and spoken) • PhD. from top University in Statistics, Operational Research, Computer Science or in a quantitative field. • 2+ years in predictive modeling and large data analysis. • 2+ years' of experience with data querying languages (e.g. SQL), scripting languages (e.g. Python, R, Scala), or deep learning libraries (e.g. tensorflow, pytorch) Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?   We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.   We are Novartis. Join us and help reimagine medicine.DivisionNBSBusiness UnitIT NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Director in PK Sciences, Biologics (80-100% )

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID279424BRPosition TitleDirector in PK Sciences, Biologics (80-100%*)Apply to Job Job Description 48! That’s the number of projects we support in the Therapeutic Area of Autoimmune, Transplantation and Inflammation (ATI) within the PK Sciences department! We provide PK and PKPD strategies from early discovery all the way through to registration and beyond. About half of this portfolio represents biologics projects spanning from classical monoclonal antibodies to complex biologics constructs. We are looking to expand our team and are specifically looking to appoint an expert group member who has the knowledge and expertise to drive our biologics projects. In your role, you will support drug discovery and development projects by providing clinical pharmacology / DMPK expertise across early and full development phases, and global medical affairs. You will represent DMPK global line function on cross-functional teams and influence design, execution and analysis of clinical pharmacology / DMPK related study components. YOUR RESPONSIBILITIES WILL INCLUDE: • Actively contribute in depth pharmacokinetic / DMPK input into key pre-clinical, clinical and regulatory documents including clinical study protocols, clinical study reports, investigator brochures, IND / IMPDs and NDA/BLAs within agreed timelines, and address all regulatory requirements in consultation with your manager • Design DMPK strategy for assigned program(s) and coordinates pharmacokinetic / DMPK related elements for pre-clinical and/or clinical projects. Identify potential project hurdles, provide solutions and establish contingency plans. Represent DMPK on Global Program Team(s) or early project teams • Responsible for the PK, PK/PD and M&S component of study protocols, reports, project summaries and development plans which meet regulatory requirements. Prepare appropriate responses to Health Authority questions (globally) • Oversee or perform PK and PK/PD analyses using a variety of tools and approaches. Integrate, interpret and report data to project teams and other customers • Ensure constructive collaboration within drug development teams (GPTs, etc.) and with other internal partners (e.g. DMPK, Toxicology, Modeling and Simulation, Formulations, Drug Regulatory Affairs, Clinical Development) • Monitor study timelines, objectives and budgets, ensure accuracy of project progress in company tracking tools (e.g. Succeed). Assure rapid and effective communication of data to project teams • Lead or participate in DMPK or project sub-teams. Coordinate with appropriate sub-team members and/or prepare summary documentation • Evaluate in-licensing opportunities and carry out Due Diligence activities as required • Ensure compliance with legal requirements and corporate guidelines (applicable GLP/non-GLP, GCP requirements) • Maintain and enhance technical and drug development expertise (e.g. training courses, external meeting attendance), and train other DMPK associates. May act as technical / scientific subject matter expert in key clinical pharmacology / DMPK related area • Attend meetings with external parties including investigators, outside mavens, and health authorities. May lead several junior associates. Coach and mentor other DMPK associates Minimum requirements WHAT YOU’LL BRING TO THE ROLE: • Ph.D. in pharmacokinetics, drug metabolism or a related discipline, or a Pharm. D. with appropriate post-doctoral training • Proficient English • 9 – 15 years of relevant post-doctoral, academic, industry or government experience • Integrated knowledge of related disciplines (i.e. DMPK, toxicology, regulatory) and the drug discovery and development process • Demonstrated expertise using in silico analysis tools (e.g. WinNonlin, Phoenix, GastroPlus, SymCyp) • Demonstrated experience and ability to work successfully as part of cross-functional teams in a highly dynamic, matrixed, project team environment • Excellent communication skills • Critical thinking and problem solving skills including publications/presentations • Strong influencing and negotiating skills • Strong coaching, mentoring and people management skills • Demonstrated leadership through involvement in external professional societies WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNIBRBusiness UnitTranslational MedicineLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Paralegal I

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID275999BRPosition TitleParalegal IApply to Job Job Description 30000+ active patent records! That’s the volume we are handling in our global R&D Intellectual Property Operations team. Would you like to join a team that is spread across 5 sites and has members from 7 countries supporting 83 Novartis patent attorneys/agents located around the globe? As part of our team based in Basel, you will support our attorneys to coordinate patent filings and patent prosecution worldwide. Your responsibilities: Your responsibilities include, but are not limited to: •Filing of EP, international and foreign patent applications and related correspondence from filing, issuance of grant and maintenance. •Responsible for meeting patent formalities requirements for EP, US and international patent filings, patent nationalizations into foreign jurisdictions and other conventions. •Responsible for draft preparation of simple responses to official communication and notifications from patent offices/agents. •Independent, proactive and critical review, maintenance and assistance of responsible attorney(s)’ dockets and ensure that all related deadlines are met in a timely manner. •Monitor and update electronic docket for responsible attorney(s) and assigned paralegal tasks on a daily basis to ensure up-to-date dockets. •Coordinate outsourcing, transfer in and transfer out of patent files and responsibilities in a timely and efficient manner, minimizing risk of loss of rights. •Maintain and share expert knowledge of latest patent rules and adapting practices to comply. •Communicate effectively with colleagues, inventors, foreign agents and other associates. •Role may include patent services data input and invoice processing. •Work within Integrity and Compliance policies and ensure those around do the same. •Work to foster a diverse and inclusive environment free from all forms of discrimination and harassment. Minimum requirements What you’ll bring to the role: • Paralegal Certificate/IP certification or a college degree in a legal discipline is desirable •English written & spoken (required) •1-2 years professional experience as a patent paralegal having worked with or managed resources from law/patent firms •ideally: exposure working in a global setting, experience of project management and governance Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. DivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

PostDoc in Immunology and Dermatology

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID279987BRPosition TitlePostDoc in Immunology and DermatologyApply to Job Job Description 1 in 10 adults in Europe suffer from autoimmune or inflammatory diseases. The Department of Autoimmunity, Transplantation and Inflammation adresses this steadily growing burden on public Health with Research in the fields of rheumatology, dermatology and beyond. We are looking for a postdoctoral fellow to investigate the biology and downstream signaling of AD-associated cytokines including IL-17C on relevant skin target cells, in human ex vivo skin biopsies and in cytokine reporter/conditional knock-out mice. We provide state-of-the-art flow cytometry, proteomics and transcriptomics as well as biochemical and molecular technologies. In-house expertise in CRISPR, immunology and translational research as well as a variety of tools to interrogate cytokine expression, and pathway activation are available. The successful candidate should have experience in use of genetically modified mice and working with primary human skin and tissues to analyze cellular and biochemical regulation of cytokine signaling and should have knowledge of immunology. Knowledge in use of CRISPR and generation and evaluation of reporter and conditional knockout mice is highly desirable. #PhD Minimum requirements What you'll bring to the role: • PhD in molecular and cell biology and/or immunology (PhD students in the last year of their thesis work, are eligible to apply) Fluency in English, Knowledge of the German language will be advantageous • Knowledge of skin immunology, translational research and/or IL-17-receptor biology are a plus • Expertise in CRISPR and transgenic mouse research are highly regarded • Expertise in bioinformatics to interrogate complex datasets would be desirable • Strong publication record • Excellent analytical, communication and organizational skills Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionNIBRBusiness UnitAUTO/TRANS/INFL - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Expert Global Trial Manager (80-100% )

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID282226BRPosition TitleExpert Global Trial Manager (80-100%*)Apply to Job Job Description 130,000! The average number of patients around the world that are actively participating in our clinical trials. As a member of our Trial Management team you will play an active role in ensuring patients have access to our clinical trials and make a difference in their lives. Your Responsibilities: • Contribute to all aspects of global clinical trial(s), under the oversight of the (Associate) Global Trial Director, to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead certain parts of global clinical trial(s). • Be a core member of the global cross-functional Clinical Trial Team (CTT); participate and report study progress and issues/resolution plan at the CTT meeting and write minutes; coordinate and chair trial sub teams within the scope of his/her delegated responsibilities. Extended member of the Global Clinical Team (GCT). • Contribute to the creation and execution of an operational risk management plan, highlighting potential risks and actions; Implement issue resolution plans and act as point of contact for all site-related issues and procedural questions, and lead interactions with relevant line functions including data management, drug supply management, clinical development and Novartis Country Organizations • Development of study tools, guidelines and training materials as well as supporting the development of Case Report Forms (CRFs), and CRF completion guidelines. Ensure trial information/documents are reported within relevant trial repositories and tracking systems • Contribute to the development of clinical outsourcing specifications to facilitate bid process and selection of Contract Research Organizations (CROs); lead interface with CROs in collaboration with outsourcing management and line functions; ensure vendors meet quality standards; contribute to the development/amendment of vendor contracts. Support the Global Trial Director with the development, management and tracking of the trial level life cycle budget. Minimum requirements What you'll bring to the role: • Advanced degree or equivalent education/degree in life science/healthcare, as well as 3-5 years of experience in clinical development with a minimum of 2 years in global clinical research (cross-functional, multicultural and international clinical trials; shown capabilities in supporting operational aspects of clinical trial related activities) • Knowledge of good Clinical Practice; comprehensive knowledge of clinical trial design; understanding of the overall drug development process • Validated ability to work either independently or in a team setting, with strong operational skills and demonstrated ability to meet goals by leading compliance, budget and timelines • Networking skills and ability to share knowledge and experience amongst colleagues • Proficient English (oral and written) and excellent communication, organization and tracking skills **Please note that for this role we are only considering applications by candidates from Basel and surrounding, close-by areas. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Scientist/Investigator I temp 80%

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80%

Back to Previous Page Job ID284765BRPosition TitleScientist/Investigator I temp 80%Apply to Job Job Description 50 human clinical trials in early phases! That is the scope of our Molecular & Cellular Sciences team in BioMarker Development / Translational Medicine. As a Scientist in Biomarker Development, you will work in close collaboration with Molecular and Cellular Sciences study leader and clinical teams to implement internal and external biomarker activities, provide interpretation of results to enable mechanistic, safety and efficacy understanding. You will be developing and validating innovative biomarker solutions, implementing new methodologies, delivering high quality data and playing a pivotal role in early phase human clinical trials. Your responsibilities will include, but not limited to: • Provide technical expertise in the field of cell based assays with a Special focus on flow, cytometry and immunoassays • Contribute to the implementation of internal and external (outsourced) biomarker activities in clinical studies • Present results at internal meetings • Implement and apply innovative biomarker solution • Conduct activities in compliance with Novartis policies, Values and Behaviour and relevant guidelines • Develop knowledge in additional biomarker modalities and/or technologies • Network internally to expand scientific and technical knowledge Minimum requirements What you will bring to the role: • BS/MS degree in Biology, Immunology or equivalent • Professional experience in the pharmaceutical or biotechnology environment, developing bioanalytical assays for soluable biomarkers • Appropriate lab experience in flow cytometry and immuno-assays • Good understanding of regulatory requirement relevant to Biomarker Development (e.g. GCP, ICH) • Demonstrable experience with any of the following: DIVA, FlowJo, FCSExpress, WATSON LIMS, SMART Book, Soft MaxPro, Spotfire, GraphPas Prism, etc. Why consider Novartis? 927 million. That is how many lives our products touched in 2017. And while we are proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you are given opportunities to explore the power of digital and data. Where you are empowered to risk failure by taking smart risks, and where people who share your determination to tackle the world’s toughest medical challenges surround you. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitTranslational MedicineLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypePart Time (80%)Employment TypeTemporaryShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Service Delivery Manager GDO Clinical Technology Innovation

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID286953BRPosition TitleService Delivery Manager GDO Clinical Technology InnovationApply to Job Job Description “165 – that’s the number of clinical projects we run across Oncology and Pharmaceuticals delivering breakthrough innovation to patients through traditional and advanced platforms. As part of the IT Clinical Technology & Innovation team this role is critical for driving key IT initiatives and managing systems that have an impact on how this industry-leading clinical pipeline is executed and benefitting 927 million lives” Represent IT to Business in Clinical Technology and Innvoation. Capture, qualify and help prioritize new IT demand. This role has to manage several concurrent high visibility projects in STRIDE Program using agile methods in a fast-paced environment that crosses multiple business areas and enable Innovation Function in Global Development Operations with powerful IT capabilities and services to create tangible business outcomes. Applying a true OneIT approach, this role will closely partner with other DIT Service Delivery teams, AMS, TIS, ISRM and critical CoEs like Robotics, Analytics and ECM You will be responsible but not limited to: • Primary point of accountability for IT matters for designated business area • Oversee IT service portfolio • Develop and enhance customer relationships • Ensure SLAs are met • Manage risks in relation to IT services • Lead STRIDE program/Projects and drive adoption of global solutions - Refine strategy for capability area • Establish relevant set of metrics to measure Progress • Effectively Managing Vendors involved in Project deliveries • Act as escalation point for all STRIDE related matters Minimum requirements • University Degree Business / Science • Fluent English • Knowledge & skills: 12+ years of business and IT experience in relevant domain. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionNBSBusiness UnitIT NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Region Europe Medical Director Multiple Sclerosis

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID287191BRPosition TitleRegion Europe Medical Director Multiple SclerosisApply to Job Job Description With a 60-year history in neuroscience, Novartis has brought innovative therapies to patients with e.g. Multiple Sclerosis, Alzheimer’s disease, Parkinson’s Disease, Epilepsy, Depression and Migraine. We have a world-class pipeline in neurodegeneration, neuro-inflammation, neuromuscular and psychiatric diseases. Our holistic R&D approach includes cutting edge molecules, innovative approaches to technology, biomarker and digital therapeutics to seek better solutions for patients. As a Region Europe Medical Director, Neuroscience, you will join a dynamic team who are dedicated to support the medical affairs task on treatments to slow the progression of degenerative diseases including Multiple Sclerosis, Huntington’s disease and Spinal Muscular Atrophy. Your role will be to lead and provide medical support to countries performance execution, strategic input for clinical deliverables or clinical sections of such deliverables in connection with Global Medical Affairs, Patients Access, Patients Advocacy, Governmental Affairs and Commercial. Your responsibilities will include: • Ensure and facilitate country Medical Affairs plans’ execution, focus on launch preparation excellence • Collation of regional specific insights where appropriate • Develop and implement lean processes that will facilitate the effective execution of medical affairs activities • Elaborate, track and analyze Regional Medical Key Performance Indicators with special focus on extent of impact on our (internal and external) Medical Experts and key stakeholders. • Commercial partnership • Identify Regional Medical Affairs capability needs and upscale through training to sustain a fully aligned, result-oriented, highly effective medical organization • Ensure excellence in stakeholder engagement to enhance collaboration and affirm Novartis as a trusted medical partner • Align Regional Medical resource deployment and budget to key regional priorities • Provide appropriate guidance on Novartis standards and policies to ensure that medical associates in the Region are ethically and legally compliant and proactively mitigate risk • Optimize or develop essential digital tools and systems that would facilitate excellence in medical execution • Facilitate the implementation of medical innovation and practice sharing • Collaborate and provide input to Region Europe Medical Plan being an active member of Europe Medical Team • Provide full support to PAM on initiatives with Patient Advocacy[#video#https://www.youtube-nocookie.com/embed/ggbnzRY9z8w{#400,300#}{#400,300#}#/video#] Minimum requirements What you’ll bring to the role: • MD, Neurology/Internal Medicine specialty will be an advantage. PhD or Pharm MD in health sciences. • At least 6 years’ experience in Pharmaceutical Industry in progressively roles with significant experience in Medical Affairs • Prior experience in country role desirable • Experience in specialty medicines and/or neurology preferred • Demonstrated inspirational leadership skills within large scientific based organizations • Strong analytical and project management skills • Experienced matrix management. • English Proficiency (oral and written), other European languages an advantage Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitREGION EUROPE GENMEDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Bioinformatics Scientist (one year contract)

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID285914BRPosition TitleBioinformatics Scientist (one year contract)Apply to Job Job Description 250 ! The number of genomics research projects that are waiting for your data analysis expertise every year. Your work will be important towards faster discovery and development of next generation breakthrough therapies for unmet medical need. The Immunology, Hepatology, and Dermatology Development Unit, within Global Drug Development is seeking a curious, talented and highly motivated bioinformatic scientists to work with the Autoimmunity Transplantation and Inflammation Disease Area at the Novartis Institutes for BioMedical Research in Basel on the analysis and integration of datasets generated as part of the Cosentyx program. As a creative and collaborative bioinformatics scientist, you will be working at the interface of the Research and Development organizations in Novartis to extract insights that further advance the Cosentyx program and related exploratory activities. Your responsibilities will include: - Analysis, integration and visualization of different types of omics data including genomics, transcriptomics, and proteomics  - Contextualization of results from omics experiments including biological interpretation, correlation with clinical endpoints and phenotypes, generation and comparison of molecular signatures, pathway- and network- level analyses  - Application of modern biostatistics and machine learning methods for supervised and unsupervised learning to heterogeneous molecular and clinical data  - Close interactions with clinicians, biologists, data scientists and business stakeholders  - Present and communicate your work to a diverse audience, contribute to the preparation of manuscripts and remain up-to-date with the relevant literature Minimum requirements What you will bring to the role: - PhD in bioinformatics, computational biology, biostatistics, biomedical informatics or a related field; Postdoc experience in academia or the pharmaceutical/biotechnology industry is considered a plus. - Excellent knowledge of computational methods for the analysis, integration and interpretation of different types of high-throughput biological data from sequencing and array-based technologies; experience with single-cell genomics is considered a plus. - Demonstrated experience with the application of supervised and unsupervised machine learning methods to biomedical data; experience with deep learning methods and frameworks is considered a plus - Excellent programming, data analysis and data visualization skills in R/Bioconductor; experience with Shiny and/or Python are considered a plus. - Familiarity with Linux/Unix command line and high-performance computing Environments. - Sound understanding of biology and immunology; Experience in working with autoimmune diseases and/or in translational/clinical research is considered a plus. - Fluent English (oral and written) Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitIHD DU GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeTemporary Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

People & Organization Internship

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Praktikumsstelle

Back to Previous Page Job ID285986BRPosition TitlePeople & Organization InternshipApply to Job Job Description More data was created in the last two years than the previous 5,000 years of human history. Here at Novartis, our vision is to become the leading medicines company in the world powered by data and digital. GDD is at the forefront of the data and digital revolution in R&D with major initiatives underway to evolve the way we discover and study potential medicines, unlocking the next chapter of medical innovation. Your responsibilities: • Responsible for handling the administrative activities as requested by HRBP • Partner with Global HRBP by preparing materials for performance / development activities and events • Collaborates with HRBP for HR cycle activities such as eComp/salary round reviews, learning nominations, reporting and data validation activities • Prepares highly confidential and accurate documentation such as mutual agreement/ severance materials and other information with strong attention to detail • Flawlessly process and validate HR Core Transactions in support of promotions, terminations, transfers and other organizational management (org-unit changes, manager changes, employment status changes) • Runs and analyzes reports for process-related data validation (calibration and compensation cycle data validation), as well as day to day activities or research (promotion population), identifying themes and trends in reports • Operational support on special projects as needed Minimum requirements What you’ll bring to the role: • Master student and / or recent master graduate (graduation not longer than a year ago) in Human Resources • Fluent in English (spoken and written), additional languages are a plus • Work experience / internship in HR are desirable • Solid written, verbal and interpersonal communication skills • Ability to adhere to the highest standards of professionalism, maintain confidentiality and consistently demonstrate sound ethics and good judgment. Excellent problem solving and multi-tasking skills • Understanding of HR processes, policies and resources that support line business partners Please apply with your CV and cover letter mentioning your availability for the position. Timing: Starting immediately Duration: 12 months Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitHR GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternship Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Senior VDO Global Program Lead

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID276839BRPosition TitleSenior VDO Global Program LeadApply to Job Job Description 30! That’s approximately the number of annual non-clinical, transformation, innovation and lighthouse programs Global Development Operations has. As a member of the Value Delivery Office, you will contribute to some of these through direct hands-on project management and implementation. In this role, you will be accountable for managing and executing programs (portfolio of projects) through expert knowledge and consultative methods, thereby enabling the organization meets its objectives. The role brings technical expertise including end-to-end project management / Lean six sigma / Agile, business transition and transformation, design thinking, solution/process design/modelling, robotic/automation/digital and consulting/facilitation support. The position also requires a leader that is able to facilitate and drive change in a heavily networked environment. Strong interpersonal, communication and networking skills are necessary, as well as an ability to make progress in an environment where there can be significant ambiguity. Key to success in this position is the ability to work within the organization at all levels, working in a “hands on” and practical way. Your responsibilities will include: 1. Program management leadership of cross-functional, strategic, high-business value projects for 2. Global Development Operations with measureable added business value outcomes and benefits 3. Drive strategic, centralized operational excellence improvement initiatives on GDD and GDO level focused on process re-engineering; producing deliverables such as the project charter, project, plan, change management plan, integrated risk register and business benefit case 4. Drive business transformation in a heavily matrixed environment 5. Apply disciplined, best-in-class project management methodologies (e.g. Agile, Scrum, or equivalent) to the delivery of complex and high visibility projects providing rigorous project planning, risk management, project controls and re-porting following Novartis Project Management framework 6. Act as Scrum Master overseeing daily standups, sprint planning, demos, retrospectives 7. Provide senior level, cross-unit and function (up to DCN - 1 level) stakeholder management to effectively manage change and proactively identify risks and mitigations 8. Understand vision, strategic imperatives, business drivers, and changing landscape. Challenge assumptions of senior stakeholders in order uncover hidden risks and build realistic plans 9. Lead cross-functional, global teams in support of initiative objectives 10. Ability to multi task and manage multiple (5+) projects at one time 11. Develop ideas for changes in process, methods, organization, location, tools and measures of success for achieving business excellence 12. Utilize process improvement methodologies and best practices (e.g. IQP, Lean six sigma, etc.) 13. Help develop and maintain core team processes 14. Prepare roadmap reports for projects to all stakeholders, including engaging with Sr. management stakeholders 15. Deputize for VDO Global Head Minimum requirements What you’ll bring to the role: • Postgraduate degree in technical or business discipline PMP, PMI, PRINCE2, SCRUM or other relevant certifications • Fluent English (oral and written) • Preferred: a second major European language • 5+ years’ experience managing teams of 10+ associates • 10+ years of project management experience, delivering cross-functional technology solutions in a variety of different styles (Agile, Waterfall, etc.) WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Reporting and Data Analytics Specialist

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID285039BRPosition TitleReporting and Data Analytics SpecialistApply to Job Job Description 105,000 unique individuals work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose; to Reimagine Medicine for millions of patients around the world The Reporting and Data Analytics Specialist will work in selected Operational Excellence and Quality (OEQ) areas associated with reporting and data analytics. The work will cover all functions within NBAA, with focus on Internal Audit. The Reporting and Data Analytics Specialist will report to the Director OEQ. You will be responsible but not limited to: • Data analytics (75%) • Facilitate promotion of OEQ driven data analytics initiatives • Generate and implement innovative ideas and creative, value added solutions that improve all stages of the audit methodology (planning, fieldwork, reporting, reviewing, and finalization). • Conduct external benchmarking of digital initiatives in audit by collaborating with other peer companies and by incorporating benchmarking thoughts, ideas and processes to continuously improve the methodology’s depth and breadth. • Contribute to data analytics projects and continuous improvement initiatives. • Manage knowledge and drive innovation to ensure high-quality, value-adding and digitally enabled audit execution. • Contribute to the digital transformation of the audit function to leverage the opportunities presented by current and new technologies and data across the organizations. Reporting (25%) • Prepare pre-defined parts of audit and quarterly reports to the Audit and Compliance Committee (ACC) and other key stakeholders autonomously. • Perform review of compliance with IA audit management tool (TeamMate) and audit practices. Suggest improvement areas, where possible, digitally enabled. • Manage preparation and communication of IA reports independently • Manage records management for IA as per compliance requirements resulting from corporate regulations (e.g. NFCM updates, Records Management, etc.) • Manage the reporting requirements to other assurance providers and open Issue Reviewers. • Support the resolution of requests associated with managing timely closure of the issues and other requests from the business Minimum requirements • Bachelor degree preferably in data science or audit • Fluent in English: oral and writing • Minimal 2 years of experience, mainly with data analytics (tools and systems). • Knowledge of AI preferred. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionCORPORATEBusiness UnitBUSINESS ASSURANCE AND ADVISORYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaAudit & FinanceJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Postgraduate Internship in bioanalytics

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Praktikumsstelle

Back to Previous Page Job ID287495BRPosition TitlePostgraduate Internship in bioanalyticsApply to Job Job Description 3! Is the number of projects you will work with during your internship. Glycans are important in modulating potency of therapeutic proteins. Most knowledge on impact of glycans on biopharmaceuticals is coming from research on the antibody’s Fc function. Aim of this internship is to extend that knowledge into emerging field of highly active therapeutic proteins. Most of the work will focus on the effects and nature of glycosylation impact on potency analysed by several in vitro as well as in vivo assay formats. Additionally, impact on protein’s PK/PD properties will be assessed. Your responsibilities: Your responsibilities include, but are not limited to: • Independently prepare and perform experiments • Prepare project reports, have excellent documentation and presentation skills • Read, prepare and discuss the scientific literature on the subject • Precision and reliability since you will be part of a GMP laboratory (internship work itself is non-GMP) Minimum requirements What you’ll bring to the role: • Masters degree in cell biology, biochemistry or relevant life science field • Excellent theoretical knowledge and strong interest in glycobiology is a must; Master thesis in this field is not mandatory but a plus • Experience with standard cell culture techniques is required; having hands on expertise on HPLC based methods is not mandatory but a plus • Strong scientific mindset with ability to work in a controlled environment requiring flexibility and adaptability Please apply with your CV and cover letter mentioning your availability for the position. As of 1st of March, 2020 Duration: 2 years Desirable requirements (optional): • English is a must, German a plus Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternship Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Cell Therapy Customer Operations Manager

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID279439BRPosition TitleCell Therapy Customer Operations ManagerApply to Job Job Description Execute a first in class order management, physician and patient care hub for Cell and Gene Therapy in Region Europe. In coordination with local country teams, Regional supply chain and selected external Partners, the Cell Therapy Customer Operations Manager ensures a seamless CTL019 process from product ordering to infusion. Major Accountabilities: - The position is responsible for enhancing the CTL019 customer experience by executing a customer centric approach to CTL019 operations management by executing support programs to health care professionals (both at infusion centers and from referring institutions), to patients and caregivers to provide a white glove service in context of a treatment with CTL019. The Cell and Gene Therapy Customer Operations Manager engages at the nexus between the manufacturing and supply functions and the patient/physician facing commercial and medical teams and is responsible for guaranteeing the timely and safe delivery of modified patient cells to patients. - Executing the first to Novartis and first in class unique HCP, Patient and caregiver Customer Services hub for CTL019 in Region Europe, to manage both commercial and clinical cases. - Supports hospital accounts across Europe in the order management process with coordination of the required logistics and delivering best-in-class customer services. - Independently drive resolution for customers by collaborating with cross functional teams and communicating with leadership as necessary. - The role works cross-functionally with the country teams, Apheresis operations, supply chain, manufacturing sites, quality assurance, legal, regulatory, marketing and medical teams to ensure that the Customer Service Center delivers against the need of our customers (both external and internal). - Provide customer service support in handling inbound customer inquiries, including telephone, email, and fax. - Conduct outbound follow-up telephone calls to ensure timely and accurate communication of information to our customers. - Implement value adding customer services to HCPs, patients and caregivers to improve their customer experience and to differentiate Novartis from competition. - Proactively work on a customer satisfaction and collect feedback, insights, and identify opportunities for improvement. - Contribute to improve and develop innovative solutions to deliver enhanced customer experience and more efficient management. - HCP point of contact for medical / technical information or side effect management and effectively identifies and processes Potential Adverse Events in accordance to Novartis training and processes. - This is a Basel based position which reports to the Director, CGT Customer Service Center. Minimum requirements - University degree in Science and/or Medical or Business (Bachelor’s Degree Minimum). - Scientific background. - Fluency in minimum three of the following languages: German, French, Italian, Spanish and English. Other European languages is a plus. - Experience in one of the following areas 1) Key account management 2)medical device key sales/account management, 3) Medical or MSL manager experience, 4) sales management experience. - Candidates could be sourced from MSL, medical, marketing, and access functions as well as commercial. - It is fundamental for the candidate to have a demonstrated ability to engage on deeply medical topics with confidence while balancing a customer oriented mindset. - Project management demonstrated experience, with ability to manage several projects in parallel. High level or learning agility and people agility. - Excellent ability to engage internal and external stakeholders at all levels with humility and a sense of urgency. - Strong communication (oral, written, and presentation) skills and ability to simply communicate complex concepts. 750million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarket AccessJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

World Wide New Products Market Access & HEOR Director, CRM (80-100%)

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID283858BRPosition TitleWorld Wide New Products Market Access & HEOR Director, CRM (80-100%)Apply to Job Job Description Decades of untapped unmet needs in the Cardio-Renal-Metabolic (CRM) space are waiting for your footprint and guidance! As part of the long-term CRM strategic and operational growth plan, this is an ideal opportunity to bring new innovative products to those in need. We seek to become the leading innovators in the CRM space by developing a transformative Precision Medicine specialty portfolio for areas of high-unmet medical need. Our new HEOR and Access Director role based in Novartis’ Headquarter, in collaboration with a very diverse team, will provide, assess and bring life-saving drugs to patients globally! Your responsibilities will include: • Provide high quality Market Access and HEOR input into the commercial assessment and strategy development for the Cardio Metabolic (CM) early product portfolio from Proof of Concept (PoC) to Full Development Plan (FDP). • Provide an integrated access & pricing strategy (for products in early development stages) aimed at delivering meaningful product differentiation and value proposition to varying payers (in terms of e.g. target patient population, clinical comparators, clinical and economic outcome measures , patient reported outcomes, health economics data, patient preferences, and diagnostics) • Work closely with the New Product Directors to ensure pricing and access strategy is aligned for submission at each development breakthrough to improve the life-time value of the brand (including existing and future evidence to rationalize and maintain price) • Lead cross-functional Value & Access Teams (V&AT) for products pre-FDP to ensure key country requirements and insights drive the commercial plan incl. payer evidence needs, plans to generate evidence (clinical, HEOR, etc.) • Represent the CM GPA input at cross franchise meetings to evaluate the access & HEOR impact for product indication sequencing. • As required support BD & L assessments as a member of Due Diligence team • Represent Global Patient Access function on the pre-FDP Global Program Teams (GPT) to optimise development program • Work closely with Patient Advocacy and the GPT team to develop a robust and consolidated Patient Engagement Plan to ensure the patient perspective is represented • Be accountable for the Market Access & Payer perspective being appropriately reflected (integrated) in the overarching product development plan for the franchise Minimum requirements What you’ll bring to the role: • Postgraduate degree in sciences, business administration health policy, plus graduate degree (Doctorate, Masters, or equivalent) in health economics, epidemiology, health services research, biostatic • 8+ years relevant market access and HEOR experience acquired at pharmaceutical companies, HTA, physician associations or health care consultancy companies • Deep understanding of payer/HTA environment and evolution across countries/regions both for hospital and non-hospital products • Ability to work and lead (a cross-functional team) in a matrix environment • Ability to communicate effectively and motivate team alongside having a persuasive and credible presentation style at all levels of organization 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarket AccessJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Post-doctoral position in biostatistics

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID278196BRPosition TitlePost-doctoral position in biostatisticsApply to Job Job Description We are looking for a post-doctoral researcher to join the statistical methodology and consulting group in GDD / Biostatistics, bringing expertise in two or more of the following areas: Computational biology and statistical genetics, applied data science and large-scale / "big data" computation, statistical and machine learning / deep learning. This position provides a great opportunity to join on-going and future industry/academic collaborations, as well as to interact with and contribute to data science initiatives in Novartis with the goal of demonstrating how new methodologies and data sources (such as genetic / omics data, imaging, time series, ...) can be brought together to gain new insights to guide drug development. Your responsibilities: Successful candidates will work in a multi-disciplinary team of statisticians, clinicians and data scientists on projects to: characterize disease progression and treatment response by integrating large clinical trial and biological datasets, demonstrate how incorporating and collecting data types such as clinical genomics or imaging add value in a drug development setting, develop new methodologies for machine learning and data analysis / bioinformatics which can be applied in a drug development setting. Start date: asap Duration: 1-2 years Minimum requirements What you'll bring to the role: • PhD in a quantitative / computational science (e.g. bioinformatics, machine learning, statistics, physics, mathematics, ...) • English written and spoken Required technical and scientific skills should include: • Strong experience with Python for data analysis (scikit-learn, numpy, Tensorflow/similar) • Experience with R for data analysis (tidyverse, mlr, ...) • Experience with computational environments for large-scale data science (e.g. high-performance computing or Spark), reproducible data science (notebooks, git/versioning, …) Additional scientific skills in one or more of the following areas are highly desirable: • Statistical and machine learning, and / or applied deep learning methods for time series data or images. • Bioinformatics (around DNA / RNA / proteomics data analysis) and/or statistical genetics Algorithms and methods for the analysis of ‘omics datasets (e.g. WGS / RNA-seq / …) Why consider Novartis: 750 million. That's how many lives our products touch. And while we're proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people's live ? We believe the answers are found when curious, courageous and collaborative people like you are empowered to as new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternship Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Global Marketing Director New Products, CRM (80-100% )

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID285067BRPosition TitleGlobal Marketing Director New Products, CRM (80-100%*)Apply to Job Job Description 1 in 5 ! That’s how many people have elevated Lp(a) and which is a today untreated driver of CV events and death. An exciting opportunity has arisen to join the Cardio Renal Metabolic Franchise as a Global Marketing Director to be part of a journey to address Lp(a) driven cardiovascular risk. This is an exciting opportunity chance to drive a complete paradigm shift in the diagnosis, and treatment of Atherosclerosis. This role will be responsible for developing and leading our global Lp(a) diagnostic strategy to achieve rapid acceleration of Lp(a) testing across priority markets to drive optimization and standardization of testing practices. This person will also shape and drive the digital strategy by leveraging AI and big data to enable the creation of predictive algorithms to identify Lp(a) patients and their physicians and use this to deliver smart target education. Your responsibilities will include: • Drive key commercial processes in alignment with the Global Brand Teams (GBT): lead and implement product strategy (integrated product strategy), competitor readiness and integrated tactical plan • Develop launch strategy in collaboration with cross-functional teams and Global, Region and Country • Lead the brand strategy plan processes and the product life cycle management discussions with a high level of autonomy • Act as commercial representative in the GPT (cross-functional Global Program Team) to co-lead or lead the commercial part of the GPT • Member of the GBT: Work closely with key functions and key Country Pharma Organizations (CPOs) to co-create commercial deliverables; drive effective communication and dissemination of deliverables to assigned CPOs and clusters • Regularly deputize the Global Marketing Executive Director when needed and act as go to person within the Franchise and the cross functional teams • Lead development of brand strategy across all customer groups and channels • Ensure alignment of Development, Regulatory, Medical, Patient Access, Digital and Patient Relation • Lead commercial deliverables / projects in co-creation with key CPOs • Provide leadership to design and delivery of marketing mix, balancing ROI with brand KPIs • Define short-term and long-term global tactics (integrated tactical plan) to support brand growth and Life Cycle Management. Collaborates with CPOs and clusters to ensure wide implementation • Lead the co-creation and launch of new campaigns that appropriately target customer groups including payors. Work closely and effectively with Medical • Design competitive simulation scenarios (as part of competitor readiness) to identify trends, opportunities and threats (worldwide and in key local markets) for product group and proposes corresponding measures Minimum requirements What you’ll bring to the role: • University degree in Science and/or degree in Business, Marketing or Clinical Research • At least 8 years of operational sales and/or marketing experience in a country with focus on extensive product/brand management including customer facing/sales and potentially market access experience • Experienced GABD and/or significant US, big EU country, or large Local affiliate commercial experience • Effective people leader with proven experiences and track records of people leadership • Have successfully and autonomously led IPS and brand strategy plan processes Desirable requirements: • Launch experience with new products or major line extensions – Cardio, Renal, Metabolic • Multi-country experience WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Global Health Insight Director

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID286061BRPosition TitleGlobal Health Insight DirectorApply to Job Job Description 90,000 are the number of patients we touch every year with our innovative Clinical Trials. In Global Development Operations (GDO) we believe we have a unique opportunity to transform clinical operations and save lives by being continuously more close to our trial participants. As part of the Transformative Business Operations team, be an actor of industry leading changes. As Global Health Insights Director you will be accountable for leading and driving data science and advanced analytics for priority business challenges across Novartis GDO with an emphasis on explorative applications of machine learning and artificial intelligence. You will infuse Patient and Site level Insights into each step of the Clinical Trial Process with focus on Feasibility, Allocation and Site Selection. Leading multi-dimentional analytics and visualization that combines real-world evidence, commercial, clinical and other competitive datasets into creative and innovative approaches. A key strategic partner to the Feasibility and Line Function teams to ensure data-supported decisions. Design and deliver user centered solutions and act as a technical expert to offer consulting and training to stakeholder groups. Your responsibilities will include: • Gain deep understanding of the domain and core processes in order to leverage Data Science to business problem solving • Generate decision-enabling information by mining complex and heterogeneous data from various sources (clinical trials, electronic health records, claims, patient registries) and technologies (omics, imaging, digital health) • Proactively work with feasibility and clinical trial teams to conduct advanced data analyses and guide the program and clinical trial decisions • Implement creative solutions to access, integrate, interpret and visualize data • Integrate advanced AI / ML, deep learning, predictive modeling and other cognitive computing methods into end-to-end business intelligence solutions. Run exploratory analytics to identify trends, patterns or process drivers • Drive the creation and execution of the data science sections of project plans for advanced analytics projects, partnering with peer Global Program Directors to contribute to the overall project strategy • Recommend and lead major process improvement initiatives or other major non-clinical project activities requiring highly advanced analytical expertise Minimum requirements Education • Doctoral or master’s degree in health related discipline • Experience providing epidemiology and/or clinical support services to medical device, biotechnology or pharmaceutical manufacturers is a plus • Masters, PhD, or equivalent experience in Life Sciences, Mathematics, Statistics, Medical Informatics, or Computer Science Experience • 10+ years of relevant experience, including a minimum of 5 years in the pharmaceutical/biotechnology industry, or a Master’s degree in Epidemiology, Public Health, or a related discipline • 7+ years of Industry experience in Predictive Modelling and Data Science in a complex fast-moving international or large national multidisciplinary data & analytics environment • Strong background in one or more of: Deep Learning, Natural Language Processing, Computer Vision, Recommendation Systems, Pattern Recognition, Large Scale Data Mining or Artificial Intelligence. • Experience with relational databases NoSQL databases such as MongoDB, Elastic Search, Redis or any graph database and fine tuning and programming experience in Python, R • Strong interpersonal and communication skills. Communicates and works with business subject matter experts and organizational leadership • Result-driven achiever with demonstrated leadership, you inspire others and build strong relationships with team members and key stakeholders • Self-motivated with a high degree of ownership and accountability for results WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Service Delivery Manager - Information Services

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID285045BRPosition TitleService Delivery Manager - Information ServicesApply to Job Job Description 20 years of untapped data waiting to be explored. The digital revolution is changing everything, especially in pharmaceuticals, and Novartis has embraced a bold strategy to drive a company-wide digital transformation. As part of the Information Security team you will be rethinking how we support this business transformation while protecting the lifecycle of physical and electronic records. You will define the Information and Records Management strategy, drive execution of priorities and translate requirements into actionable plans. Also you will oversee the Books & Records operations for the company and provide guidance on the lifecycle of physical and electronic Records in the context of Mergers & Acquisitions and Divestitures. Responsibilities include: - Act as primary point of accountability for respective service matters for business or IT customers usually across locations, business domains, and/or geographical boundaries - Develop and enhance relationships with key stakeholders, actively manage their expectations and monitor satisfaction levels and service adoption - Lead management of day to day service operations and ensure resource efficiency - Manage a global team of internal and external resources - Develop standards and best practices to deliver services (e.g. for Transactional Service Agreements) - Ensure the overall user experience is taken into account when designing and deploying new services - Identify root causes of problems and initiate fixes required to prevent recurrences - Ensure Records Management Framework is appropriately maintained, updated and amended to reflect changes, trends covering paper and electronic data (structured, semi-structured and unstructured) - Establish close collaboration with corporate compliance stakeholders to facilitate alignment with other policies and processes - Interact with internal and external security and compliance experts to identify industry trends Minimum requirements Desirable qualifications: - Over 5 years of professional experience in a similar or related role - Masters level degree in business/technical/scientific area or comparable education/experience - Experience with M&A transactions, vendor negotiations or comparable. - Knowledge in any of the following a plus: IT compliance, risk management, SOX IT, GxP / e-compliance, Data Privacy, Legal Hold, eDiscovery, etc. - Business fluent in English (written and spoken) - Experience in reporting to and communicating with C-level management - High level of personal integrity, and the ability to professionally handle confidential matters - High degree of initiative, dependability and ability to work with little supervision. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionNBSBusiness UnitIT NBSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Expert Regulatory Writer (80-100% )

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID274930BRPosition TitleExpert Regulatory Writer (80-100%*)Apply to Job Job Description 200+ projects in development. 20 major approvals. 20 major submissions. And that’s just in 2018. This is your chance to help reimagine medicine in 2019 and beyond. Novartis is looking for dedicated individuals to join our Regulatory Writing team and contribute to developing our pipeline of drugs and biologics into innovative therapies for our patients worldwide. Read on for details about the role and how you can join a world-class organization at the forefront of the industry and how you can further your career. In this role, you will write, review and/or manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. You will provide authoritative documentation-related consultancy to other line functions. You will coach/mentor and/or train less experienced writers. Your responsibilities will include (but are not limited to): ∙ Author, review and/or independently manage high quality clinical and safety documents for health authorities. ∙ Lead writing team for complex submissions, actively contributing to key messaging and pooling strategy, providing expert content guidance for) clinical submission documents, contributing to statistical analysis plans and presentation of outputs, and ensuring compliance of documentation to internal company standards and external regulatory guidelines. ∙ Program Writer for large and/or complex programs ensuring adequate medical writing resources are available for assigned program and consistency between documents. ∙ Lead process improvement in Regulatory Writing and Submissions and cross-functional initiatives and/or activities. ∙ Coach and/or mentor less experienced writers. Minimum requirements What you’ll bring to the role: ∙ ≥ 6 years medical writing experience or other relevant pharma industry experience combined with scientific and regulatory knowledge, plus expert knowledge of medical writing processes ∙ Expert knowledge of the global registering of drugs, and extensive experience and demonstrated record of accomplishment of leading complex submissions. ∙ Fluent English (oral and written) and excellent communication skills ∙ Proven ability to prioritize and manage multiple demands, projects and cross-functional teams. ∙ Future-oriented perspective and demonstrated ability to define and solve complex problems. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Senior Global Trial Manager (80-100% )

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID282222BRPosition TitleSenior Global Trial Manager (80-100%*)Apply to Job Job Description 130,000! The average number of patients around the world that are actively participating in our clinical trials. As a member of our Trial Management team you will play an active role in ensuring patients have access to our clinical trials and make a difference in their lives. Your Responsibilities: • Contribute to all aspects of global clinical trial(s), under the oversight of the (Associate) Global Trial Director, to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). • Be a core member of the global cross-functional Clinical Trial Team (CTT); participate and report study progress and issues/resolution plan at the CTT meeting and write minutes; coordinate and chair trial sub teams within the scope of his/her delegated responsibilities. Extended member of the Global Clinical Team (GCT). • Implement issue resolution plans and act as point of contact for all site-related issues and procedural questions, and handle interactions with relevant line functions including data management, drug supply management, clinical development and Novartis Country Organizations • Development of study tools, guidelines and training materials as well as supporting the development of Case Report Forms (CRFs), and CRF completion guidelines. Ensure trial information/documents are reported within relevant trial repositories and tracking systems • Contribute to the development of clinical outsourcing specifications to facilitate bid process and selection of Contract Research Organizations (CROs); lead interface with CROs in collaboration with outsourcing management and line functions; ensure vendors meet quality standards; participate in the development/amendment of vendor contracts. Support the Global Trial Director with the development, management and tracking of the trial level life cycle budget. Minimum requirements What you'll bring to the role: • Advanced degree or equivalent education/degree in life science/healthcare, as well as 2-4 years of experience in clinical development (cross-functional, multicultural and international clinical trials; confirmed capabilities in supporting operational aspects of clinical trial related activities) • Knowledge of good Clinical Practice; comprehensive knowledge of clinical trial design; understanding of the overall drug development process • Shown ability to work either independently or in a team setting, to meet goals by leading compliance, budget and timelines • Validated networking skills and ability to share knowledge and experience amongst colleagues • Proficient English (oral and written) and excellent communication, organization and tracking skills **Please note that for this role we are only considering applications by candidates from Basel and surrounding, close-by areas. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Postgraduate Program BMD

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID286682BRPosition TitlePostgraduate Program BMDApply to Job Job Description 6000! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Novartis Institutes for BioMedical Research (NIBR) is the global pharmaceutical research organization for Novartis committed to discovering innovative medicines that treat disease and improve human health. BMD post-graduate is part of Laboratory Excellence and Operation team in Biomarker Development which provides operational and CRO assay support for clinical studies. Your responsibilities: • Gaining familiarity with a wide range of innovative biomarker platforms and laboratory technologies used in clinical research. • Develop and provide operational review of study protocols, site operations manuals, biomarker sample logistics including study setup, sample tracking/reconciliation, and data upload. • Perform logistical and operational activities for soluble (ELISA and LC-MS), cellular (FACS) and other biomarkers, coordinating with clinical sites, managing and tracking material supply and sample at sites, central lab, and CROs • Monitor and provide oversight of BM modalities and laboratory assays (e.g. flow cytometry, Immunoassays) and coordination activities as assigned • Collaborate with BMD internal functions, clinical teams, CROs clinical trial leaders to trouble shoot and resolve issues related to biomarker monitoring as well as drive biomarker implementation in clinical studies • Provide training to clinical sites / external service providers when needed • Leading process improvement projects, technology evaluations/implementation and other initiatives across NIBR sites. Minimum requirements What you'll bring to the role: • Recent postgraduate degree in a Scientific field: PhD or PharmD • Fluent oral and written English • Previous laboratory experience in Biomarker analysis technique (LC-MS, Immunoassays, Flow cytometry Please apply with your CV and cover letter mentioning your availability for the position. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionNIBRBusiness UnitTranslational MedicineLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Director, Scientific Communication

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID270951BRPosition TitleDirector, Scientific CommunicationApply to Job Job Description 4,000, the number of publications in peer-reviewed journals and at medical congresses Novartis Oncology has published and presented over the last 10 years. As Director, Scientific Communication, you will be accountable for the strategic direction and execution of Pipeline scientific communications for Phase 1/2 product(s), including alignment with Novartis Institutes for BioMedical Research (NIBR) Translational Clinical Oncology (TCO), Oncology ECS, and Oncology Medical Affairs (OMA) by collaborating on data interpretation, publication of key results, and delivery of pipeline medical education for key translational programs. You will function as a participant in the Scientific Engagement & Communications (SEC) Leadership Team, supporting overall strategic direction and priority focal areas for global Scientific Engagement and Communication department. Your responsibilities will include: 1. Accountable for all aspects of scientific communication strategies for assigned Early Asset Oncology products directly and/or indirectly including: • Leading a cross-functional publication team and developing publication plan/s (GMA, TCO, ECS, Legal/Regulatory) for key select pipeline compounds • Leading development of a comprehensive communication strategy/plan with related Pipeline content resources/platforms in alignment with GMA, TCO/EPTs and/or ECS team (medical/commercial/regional) • Establishing strong working relationships and actively collaborating with key internal and external stakeholders (GMDs, ECS, TCO, Oncology Corporate Communications, NIBR Communications, US Sci Comm team, medical experts, speakers, consultants, and professional societies) • Ensuring alignment of global medical education needs with regional/country needs • Managing all aspects of publication and medical education agencies in support of scientific communications. Identifying and screening appropriate vendors, soliciting, evaluating and approving proposals 2. Responsible/accountable for congress scientific communications including: • Data interpretation in collaboration with GMD / ECS team on both internal trial results and key competitor data • Developing internal global communications and education for Novartis products Presentation to upper management, regions & CPOs 3. Participating in SEC department Leadership Team to manage across the full portfolio of products / disease states & franchises including: • Providing strategic direction input to Leadership Team on an ongoing basis • Ensuring business needs and annual objectives are met • Recruiting and hiring support • Onboarding and training support • Mentoring, coaching, performance management 4. Initiating and sponsoring functional excellence enhancement projects to drive long-term medical education and publications excellence across entire department / organization 5. Leveraging established relationships with medical experts, functioning as respected company representative to medical experts 6. Reviewing and approving all financial and contractual aspects of assigned budgets, including managing monthly spend within budget, overseeing the development of yearly budget for entire team across multiple products / diseases / franchise. Helping to co-manage whole department budget Minimum requirements What you’ll bring to the role: • Advanced scientific degree (PhD, PharmD, or MD) • Business-level English • 7+ years’ experience in pharmaceutical industry or healthcare related, ideally in Medical Affairs publication planning and/or medical education activities • 3+ yrs Oncology related experience (preferred) • Experience in the development of communication strategies & key scientific platforms • Ability to provide strategic insight into scientific expert development activities, publication planning plus developing medical education materials and programs that support product launches in oncology • Proven record of accomplishment in a Scientific Communications role including interpretation and presentation of complex scientific data • Strategic mindset including innovation and critical thinking with performance-oriented drive • Experience in planning and executing live educational events and enduring materials and/or experience in driving the development of scientific messaging and execution of publications preferred • Expert project management and budget management experience WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Strategic Program Director, data42

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID277624BRPosition TitleStrategic Program Director, data42Apply to Job Job Description data42 is Novartis’ transformational program to leverage 2 million patient-years of data in one of the largest and most diverse datasets in the pharma industry, with the ultimate moonshot goal to change the way we develop medicines. At Novartis, we believe that Artificial Intelligence combined with the wealth of our data and internal scientific expertise will transform life sciences. In our Executive Committee-sponsored program, we operate like an internal start-up to get more medicines to more patients faster by (1) making internal and external data machine learnable and (2) applying advanced analytics to derive insights that contribute to (3) increasing our understanding of the disease and medicine thereby (4) enhancing R&D decision-making With data42, we will deliver more value to patients while building a competitive edge for Novartis R&D The Strategic Program Director, data42 will have responsibilities for end to end delivery of enterprise wide big data and analytics platform called as data 42. Lead external engagements and partnerships for advancing the platform and analytics, define program vision and priorities (Annual and long term). Work closely with key stakeholders to align expectations and ensure full support from the organisation. Build strategy for adoption and growth of the platform. Support in building momentum across the organisation. Define key priorities and success metrics for the program in alignment with executive sponsors. Support in achieving KPI’s. Review overall spend, contracts, expenses, resources and suggest required actions for optimum and efficient use of the budget. You will be responsible but not limited to: Program Strategy • Build the long term Data42 program strategy taking into account internal and external considerations. • Ensure effective implementation of long term strategy by closely working with product teams and LT members External Advisory Board • Own and manage the external advisory board for data42. Define charter, purpose, cadence, membership and perks. • Organize and run the external advisory board. Act as Board secretary. Ensure the meeting is productive, with right attendees. Drive Strategic projects • For strategically important projects drive project teams to solve complex problems • Creates a structured program framework; able to deal with ambiguity, highly autonomous and able to report on program progression • Ensures the delivery and implementation on target, within budget and on time • Accountable for cross-functional alignment and organizational support of the projects by facilitating internal and external stakeholder management Strategic Advisor to Program Sponsor and Head • Advise Program Sponsor and Head on various strategic matters of importance.Take on ad hoc strategic task’s and projects to support Program sponsor vision along with Program Head.. Minimum requirements • Bachelors/Master’s degree in scientific/technology discipline from top-tier university with consistent outstanding academic record. • Past experience in entrepreneurship is highly desirable. • Fluent oral and written English • 8+ years of relevant experience in a multidisciplinary environment or in a line function (drug development) • Consulting background is highly desirable • Strong Biology, data and analytics background • Location can be either in Switzerland, US or UK Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkYes Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Principal Biostatistician (80-100% )

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID278597BRPosition TitlePrincipal Biostatistician (80-100%*)Apply to Job Job Description 200+ compounds in Novartis are supported by biostatisticians in 10+ sites around the globe. Biostatisticians transform clinical data into analyses that build the basis for making innovative drugs accessible for patients. They influence decision-making in cross-functional international teams from early to late phase drug development. As Principal Biostatistician you will be responsible for all statistical work, scientific and operational, for one or more assigned trials in collaboration with the clinical trial team. You also may support project level deliverables for a development project. You will drive the implementation of modern and innovative clinical trial/experimental designs, statistical models, analyses and data exploration at the study level. Your Responsibilities: • Responsible for all statistical tasks covering planning, reporting and data exploration activities on assigned clinical trial(s) and perform these tasks independently with peer input and/or alignment with Lead Statistician. • Implement innovative trial designs in clinical trial protocols, ensure protocol development in alignment with the overall drug development strategy. • Represent Biostatistics on cross-functional international teams for the assigned trial(s) and collaborate with other line functions. • Explain statistical concepts and analysis results in manner easily understood by non-statisticians and provide adequate statistical justifications for actions/decisions/statements when required. • Provide statistical expertise to support the submission of a new drug and other drug development activities, as required. Minimum requirements What you’ll bring to the role: • Principal Biostatistician: MS (in Statistics or equivalent) with 4+ years relevant work experience or PhD (in Statistics or equivalent) with relevant work experience (including internship). • Fluent English (oral and written) • Proven knowledge and expertise in statistics and its application to clinical trials, able to explain statistical designs and concepts. • Depending on the assignment, may require expertise in applied Bayesian statistics, and/or data exploration skills. • Proficiency in use of statistical software packages (e.g. SAS or R). • Good knowledge of drug development and Health Authority guidelines. • Good communication & presentation skills, collaborator in multidisciplinary teams • Influences decisions that directly impact the assigned clinical trial(s) and team ability to deliver objectives. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. ** Please note that for the particular role, we will only be able to process applications of candidates who have an EU/EFTA Passport, a Swiss Passport, or a Swiss residence/work permit.DivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Automation Scientist (80-100% )

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID284559BRPosition TitleAutomation Scientist (80-100%*)Apply to Job Job Description 280 + curious minds! That’s the number of scientists in Novartis Biologics Center who daily work in our labs to make a difference in patients’ lives. We are seeking a motivated and experienced automation scientist. As a scientist in the automation team inside the antibody discovery group you will be developing, validating and performing high throughput assays on all automated systems as well as executing screening campaigns for antibody discovery. In addition, this role requires hands on experience of automated bioinformatics analysis tools and programming languages. Your responsibilities will include but are not limited to: • Plan, run and troubleshoot processes on automated systems • Assume ownership of assigned automated systems for maintenance, repairs and readiness state in compliance with internal regulations • Analyze run data generated on automated systems using KNIME workflows and relational database system • Create or modify data analysis workflows for effective flow and data management • Contribute to cross functional automation projects by collaborating with other associates Minimum requirements What you will bring to the role: • Master’s degree in Biology, Biochemistry or Engineering or equivalent experience in industry • 5+ years experience in laboratory automation, preferrably in a biologics/ antibody discovery environment • Experience with biochemical assay formats such as ELISA • Proven track record in developing processes on Tecan or Beckman- Coulter liquid handling platforms including scheduling software (SAMI, Evoware Plus) • Hands- on experience with data management/ analysis software such as KNIME or Spotfire • Working knowledge and high motivation to use at least one of the following: R, Python, Visual Basic script, Java script or SQL Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNIBRBusiness UnitBIOTHERAPEUTIC AND ANALYTICAL TECHNOLOGIES - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Global Program Safety Lead

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID282844BRPosition TitleGlobal Program Safety LeadApply to Job Job Description 1 in 8. Almost one in eight women will be directly confronted with breast cancer at some time during their lives. As a Global Program Safety Lead in the Breast Cancer group at Novartis, you will join a team of experts who are working to positively transform the lives of patients living with this disease. In this role, you will successfully serve as scientific safety leader to improve patients’ lives and impact on overall Novartis results through robust safety evaluation expertise and medical innovation. Your responsibilities will include, but are not limited to: • Providing expert safety input to the clinical development program for assigned projects/products, contributing as an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT) • Safety issue management from formation of Global Program Team (GPT) through all stages of Life Cycle Management • Developing and responsibility for key internal Novartis safety documents; reviewing these documents regularly and updating as required, ensuring that these, and all other project-related safety documents, are consistent in message • Owning the safety strategy and recording appropriately in the corresponding documents (e.g. dSPP, SSPT). Leading the production of the medical safety deliverables (e.g. DSUR, PSUR, RMP) for assigned products • Responsibility for overall signal detection, monitoring, evaluation, interpretation and appropriate management of safety information based on input from all relevant line functions, post-marketing and other data sources. Running the Safety Management Team (SMT) and ensuring that the team reviews all medical safety data throughout the development and post-approval process in an appropriate and timely manner • Responsibility for responding to enquiries from regulatory authorities or health care professionals on safety issues. Leading the preparation of the safety strategy for health authority responses and strategy, in collaboration with other project team members Minimum requirements What you’ll bring to the role: • Medical Degree (MD) or equivalent preferred. PhD or PharmD with 3 years clinical experience • At least 5 years’ experience in drug development at a major pharmaceutical company, of which 2 years will ideally be in a global position • Minimum 2 years of Safety experience in an operational or medical position • Experience in preparing or contributing to the preparation of clinical safety assessments and regulatory reports / submissions involving safety information • Experience in leading cross-functional, multi-cultural teams WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitCMO & PATIENT SAFETY GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Analytical Project Leader, Technical Research & Development (80-100% )

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID282135BRPosition TitleAnalytical Project Leader, Technical Research & Development (80-100%*)Apply to Job Job Description 90! The number of New Molecular Entities currently in clinics awaiting to be transformed into successful high quality innovative medicines and in need of Analytical Project Leaders in charge of the development of analytical control strategies throughout development, from the time they leave the discovery laboratory until the transfer to commercial production. As part of the Analytical Research and Development group, this is a new role waiting for you to put your own stamp on it. The position is located at the Novartis Headquarter site in Basel within the Technical R&D (TRD) department of Global Drug Development. Your responsibilities: • Developing and driving the overall analytical project strategy (API and formulated drug product, essentially small molecules) • Leading and managing all analytical activities within a global project team (e.g. specification setting, method development and validation, stability and release testing) • Accountability to meet quality, timelines and budget for assigned projects, defining analytical project plans • Managing interactions with internal and external stakeholders, including potential outsourced activities • Proactively identifying potential scientific, technological and GMP gaps, proposing creative solutions and ensuring appropriate communication within and across units • Providing input into CMC documents to support regulatory submissions • Strong contribution to advance science, technology and innovation within ARD Minimum requirements What you’ll bring to the role: • Minimum BS / MS in analytical chemistry with significant experience in industry, PhD in analytical chemistry or equivalent desirable • Minimum 3-5 years’ experience in the pharmaceutical industry, preferably in analytical development or quality control • Proven leadership experience in managing projects ideally in a global matrix environment • Strong quality focus, experience in a GMP environment • Understanding of regulatory expectations and profound scientific knowledge in analytical development • Fluent in English (oral and in writing), German desired • Ability to perform in a highly dynamic environment Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Real World Evidence Scientist (80-100% )

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID276057BRPosition TitleReal World Evidence Scientist (80-100%*)Apply to Job Job Description 21st Century evolution and innovation in digital technologies, data and advanced analytics is rapidly changing the healthcare environment. We believe that Real World Evidence will transform healthcare decision-making as part of that revolution. As a Real World Evidence (RWE) Scientist within the RWE Center of Excellence (CoE), you will be responsible for developing RWE strategies that deliver innovative and scientifically robust evidence. You will collaborate with multiple stakeholders and partner throughout the organization to design RWE studies and implement analyses to address product- and disease-area research questions, which will inform business decisions about the research and development of our products as well as support healthcare decisions by patients, physicians, health authorities, payers, and policy-makers. This will require a deep understanding of observational research methods to define appropriate research questions and data sources, study design, rigorous and fit-for-purpose analytical approaches as well as strong communication skills to summarize and present findings. You will need excellent technical, strategic, leadership, collaboration and communication skills, as well as an entrepreneurial mindset, to work with and through others, to reimagine the way we use data and analytics to develop and deliver medicines for patients. As a RWE Scientist, you will drive the development of RWE approaches, techniques, and standards using your expertise in an assigned area in the Oncology Business Unit. You will work closely with franchises in regions and key countries to enable RWE and sharing of best practices across geographies. Your responsibilities will include: • Develop and drive RWE strategies, in collaboration with internal partners, to ensure that the value of our medicines is fully supported by evidence both globally and locally • Lead cross-functional Real World Evidence team consisting of internal partners with the clear objective to deliver scientifically valid and robust evidence to support all stages of product development, and to drive global and local value demonstration • Ask the right scientific questions, understand the evidence needs for product development, regulatory and market access, and ideate and make recommendations on fit-for-purpose data and analytics solutions • Work closely with regions and countries to develop timely, meaningful and robust evidence to support product value demonstration aligned with local needs (patient access, reimbursement, medical education, and patient advocacy) • Foster learning with internal and external partners by using analytical tools and applications to broaden data accessibility and advance our proficiency/efficiency in understanding and using the data appropriately • Stay current with and adopt emergent analytical methodologies, tools and applications to ensure fit-for-purpose and innovative approaches • Apply rigor in study design and analytical methods; design a fit-for-purpose analysis plan, assess effective ways of presenting and delivering the results to maximize impact and interpretability; implement and/or oversee the study, including its reporting; ensure compliance with applicable pharma industry regulations and standards • Communicate findings to internal stakeholders, regulatory, health technology assessment (HTA) bodies and scientific communities; publish results; participate in external meetings and forums to present your insights (e.g. congress/conference) • Collaborate and contribute to functional, cross-functional, enterprise-wide or external RWE communities, networks, collaborations, initiatives or goals on knowledge-sharing, methodologies, innovations, technology, IT infrastructure, policy-shaping, processes, etc. to enable broader and more effective use of data and analytics to reimagine cancer treatment • Provide expert input to evaluate external technologies or capabilities in data and analytics according to their strategic fit to the business and priorities Minimum requirements What you’ll bring to the role: • Advanced degree or equivalent education/degree in life science/healthcare required. PhD or equivalent preferred • Fluent English (oral and written) • 5+ years relevant experience acquired at pharmaceutical companies, academia, healthcare provider / Payer / HTA, or relevant consultancy companies • Deep understanding and experience of Real World Data/Real World Evidence or related disciplines to generate scientifically rigorous and value evidence from secondary data sources • Strong understanding of drug development with proven ability to identify and deliver key evidence needs for Clinical Development, Commercial, Market Access, HEOR, Medical, Safety, Regulatory stakeholders • Demonstrated track record of leading and execution of research projects using real world data from claims, electronic health records, registries, biobanks, or digital applications, including publications • Experienced and with a strong knowledge of observational and/or epidemiological research methodology and statistical methods • Demonstrated experience with managing project scope and driving delivery in a fast evolving environment WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarket AccessJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Real World Evidence Data Scientist (80-100% )

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID277015BRPosition TitleReal World Evidence Data Scientist (80-100%*)Apply to Job Job Description 21st Century evolution and innovation in digital technologies, data and advanced analytics is rapidly changing the healthcare environment. We believe that Real World Evidence will transform healthcare decision-making as part of that revolution. As a RWE Data Scientist, you will work with meaningful data to gain impactful insights on our medicines and patients. The data will be varied in type -- patient-level clinical data, supplemented with deep patient data like genomics, imaging, digital health, etc. Source data will be diverse -- real-world data, including patient registries, electronic medical records, claims and biobanks. The RWE Data Scientist will be responsible for contributing to and executing the RWE strategy within Novartis Oncology. This role will partner with RWE Directors, Scientists and cross-functional stakeholders to translate real world data into evidence and insights. You will work collaboratively to build strong internal partnerships and act as subject matter expert by providing expert consultations on all aspects of RWD studies and analyses, including objectives, study design, data source identification, protocol development, statistical analysis, and/or interpretation. Furthermore, you will be responsible for implementing RWD-based analyses using programming and rapid-analytic tools. You will bring an innovative mindset and fresh perspective to the use of data and analytics in oncology and be a key contributor to improving analytic efficiencies and expanding the use of RWE across the organization. Your responsibilities will include: 1.Partner with RWE Directors, Scientists and x-functional stakeholders to develop a deep understanding of evidence needs and to conceptualize and implement RWD-based analyses and studies 2.Support the development of real world data and analytics capabilities and utilization, and lead in applying cutting-edge advanced analytics methodologies and tools to generate novel insights and actions 3.Conduct and oversee execution of RWD-based queries and studies; effectively communicate the findings and study results to internal stakeholders 4.Ensure high quality, rigorous and readily interpretable deliverables are generated from RWE studies/analyses 5.Build RWD-based self-service analytic tools that will enhance analytic efficiencies and will expand the use of RWD/RWE across the entire product life-cycle 6.Support the incorporation of RWE methods and perspectives into global development strategies 7.Continuously improve the data analytics platform, creating industry-leading performance through leveraging new and creative data sources and collaboration models with third party networks 8.Define standards and processes to manage quality, consistency, usability, security, and availability of data throughout the data lifecycle 9.Develop and address opportunities around novel sources or applications of data, and define how the business creates additional value through utilization of real world data and analytics, and drive cultural change towards data and analytics centricity 10.Improve literacy in the value and use of data and advanced analytics across the organization by leading successful implementation of data and analytics initiatives across regions and countries 11.Manage external data and analytic partners and collaborate closely with other analytic teams across Novartis 12.Define functional objectives as well as KPI and quality metrics, identify opportunities, gaps and priorities, and contribute to best practices standards. Stay abreast of emergent applications and positively drive development of RWD and analytic capabilities globally and locally Minimum requirements What you’ll bring to the role: • Advanced degree or equivalent education/degree in life science/healthcare required (e.g., biostatistics, epidemiology, bioinformatics, computer science, mathematics, data science) • Fluent English (oral and written) • 7+ years relevant experience acquired at pharmaceutical companies, academia, healthcare provider / Payer / HTA, or relevant consultancy companies • Extensive experience with analytics, including statistical programming languages (SAS, R, Python); experience with rapid analytics platforms such as IHD and producing interactive outputs is a plus; • Experience with technologies to undertake analyses on large data sources or with computation-ally intensive steps (SQL, Hadoop, Spark) • Experience producing interactive outputs (Shiny etc) • Contributor to open source packages, libraries or functions • Experience implementing reproducible research practices like version control (e.g. using Git) and literate programming • Deep understanding and experience of Real World Data/Real World Evidence or related disciplines to generate scientifically rigorous and value evidence from secondary data sources • Awareness of changing analytics and technology trends within and outside the industry WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionOncologyBusiness UnitONCOLOGY BULocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarket AccessJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Intern, Postgrad, PhD Student, Post-Doc Biostatistics

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Praktikumsstelle

Back to Previous Page Job ID284877BRPosition TitleIntern, Postgrad, PhD Student, Post-Doc BiostatisticsApply to Job Job Description 700 ! The number of days we can get therapies faster to patients applying technology innovation. The internship will focus on the development and/or application of statistical methods in clinical research and development. Mathematical, statistical, graphical or programming techniques will be used for data analysis, simulation and display. This internship will provide motivated postgrads, PhD Students and Post-Docs with an exposure to pharmaceutical industry and with the opportunity to work in an exciting, multi-disciplinary and multi-cultural environment with senior-level biostatisticians. The intern will also be able to participate in a variety of educational opportunities within the biostatistics function of the Integrated Quantitative Sciences (IQS) department. The internship is expected to last approximately 3 months, or up to 6 months. Minimum requirements The candidate should be familiar with common statistical methodology and be interested in its application in drug development. Good written and oral communication skills in English are required. Programming skills in a statistical programming language such as SAS or R are expected. The candidate should hold a Master’s Degree, PhD or equivalent in Mathematics, Statistics, or related subjects, and be enrolled in a corresponding PhD program. Language: English Duration: 3-6 months Why consider Novartis ? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitCD&A GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternship Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

TMF Repositories Support Lead

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID275647BRPosition TitleTMF Repositories Support LeadApply to Job Job Description 20 +! This is currently the approximate number of TMF systems or repositories at Novartis. As TMF Repositories Support Lead, you will act as business lead for integration and interfaces of TMF repositories and support improvements and innovation on business and technical aspects of document management and archiving, including implementation of innovative methods. Your main responsibilities will include, but not limited to: • Ensure as a Business lead that assigned systems/tools (e.g. VirtualTOC, eTMF4 etc) can support Clinical Trial Teams and inspector/auditor activities. • Provide support before, during and after audits and inspections on questions related to TMF systems, tools and processes. • Support the strategy for integration and/or interfaces of identified TMF repositories with the new Document Management System and assess future systems functionalities to ensure compliance with regulatory requirements. 1) Maintain and implement the plan for integration and or interfaces of identified TMF repositories into the new Document management System. 2) Ensure compliant storage of TMF documents/data in Novartis by developing and supervising trainings courses, migration procedures and processes. 3) Contribute to the implementation of global plan for archiving the electronic TMF documents authored/imported in the different Novartis Systems. • Support future releases of new document management system by providing direct input to the user requirements, change requests, file plan, migration, testing and deployment • Support enhancement of TMF documents/data access throughout the company and for inspections, • Act as a Core member of the TMF Governance Team for any TMF related questions and supporting procedures, guidelines and tools update/creation. Minimum requirements What you’ll bring to the role: • College degree or equivalent education in life science/healthcare or related scientific discipline (natural, pharmaceutical, medical, archival or information technology). • Fluent English (oral and written) • At least 5 years of relevant experiences in managing, archiving, retrieving or compiling clinical documents / At least 6 years of relevant clinical research/pharmaceutical industry experiences • Lead Expert in electronic Trial Master File systems and Archiving • Good organizational and IT skills and significant project work or project management experience Additional requirements: • Experience with stakeholder management in a matrix organization. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

MD PhD Immunology Data Science Expert, Translational Medicine

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID272657BRPosition TitleMD PhD Immunology Data Science Expert, Translational MedicineApply to Job Job Description 20 petabytes of data. 2 million patient-years of information. 30 data domains from preclinical through Phase 3 trials. All waiting for you to unlock the next breakthrough in medicine. Novartis Institutes for Biomedical Research is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Not only do we fund the majority of our own internal discovery research, the way we approach it is different too: partnering physician scientists with basic researchers and data analysts enables us to focus earlier on unmet patient need and discover where drugs will have the most impact. Translational Medicine is a group of physicians and scientists that drive innovative science from discovery to the patient through the selection, profiling, and effective development of medicines. As a Translational Medicine and Data Science Expert you will provide medical and scientific expertise and leadership to: • Drive the success of early global programs, develop and implement strategies to achieve clinical Proof of Concept as well as late global programs; and develop and implement strategies leading to clinical pharmacology and profiling packages that meet regulatory requirements and support differentiated and competitive drug labeling • Support Translational Research in developing new indications, endpoints and biomarkers, using in vitro, in vivo, or in silico methods • Apply data science methodology to identify potential indications, endpoints, biomarkers, and pathway nexi that can optimize the early clinical development strategy by collaborating with the Biomarker Development team and research discovery colleagues to integrate clinical and preclinical information into the clinical development approach. • Apply data science methodology to develop evidence to support the full development program. This includes using internal and external data to evaluate the impact of various clinical scenario • Provide leadership between medical and data science disciplines to leverage Novartis and external data for Translational Medicine programs. • Provide scientific expert assessments and support for in-licensing opportunities, including due diligences You will join at an exciting time for Data science programs in Novartis, including one that’s digitizing all the clinical and preclinical data collected since our inception to create a single accessible, searchable database that will transform how we do research. Minimum requirements What you will bring to the role: • Medical Doctor degree required; additional PhD / PhD-level research. Board Certified preferred • Demonstrated clinical background and patient experience in one or more of immunology, allergy, dermatology, rheumatology, renal or transplant. • Relevant scientific excellence, evidenced by quality publications and significant contributions to your field over time • Quantitative expertise in biostatistics, bioinformatics, computer science, data science or related technical field. Hands-on experience analyzing, interpreting, publishing studies consisting of a variety of omics technologies (NGS, proteomics, etc.). Formal training and demonstrated experience with machine learning, “big data” analysis, statistical approaches to exploratory analysis, or related aspects of data science • Experience performing in a similar role within a Pharmaceutical research company, a Clinical Research Organization or an academic medical center. Used to leading complex cross-functional/matrix project teams with proven success collaborating with expert disease research scientists and non-specialists • Recognized expert in your field. You have driven success for studies and projects and are respected by a wide range of internal colleagues and external collaborators • Demonstrated passion for science, seeking out new clinical discovery opportunities and early clinical study approaches • Advanced leadership, planning, prioritization, problem solving and organizational skills • Business-level/fluent English Novartis supports international family relocation. ABOUT TRANSLATIONAL MEDICINE Translational Medicine (TM) is a global group of nearly 900 scientists and physicians working at the pre-clinical and early clinical stage of drug discovery. Our Physician-Scientist TM Discovery & Profiling group drives innovative and cutting–edge science from Discovery to the market through the selection, profiling and effective global development of successful medicines. The group closes the gap between preclinical research and clinical development and integrates clinical science into the discovery and preclinical development phase. Our Translational Medicine concepts are driven by medical needs of the patient and the concept of personalized medicine, tailoring the drug, its dose and dosing regimen to the patient that the clinical response is optimal in efficacy and safety. We focus from identification of drug targets (molecular pathways relevant to disease) up to the completion of Proof of Concept (Phase IIa studies). Our Translational Medicine Experts are part of preclinical project teams in all drug discovery phases and help design the pathway for First in Human studies (healthy volunteer) that bridge to studies in the patient population. They have the comprehensive responsibility for designing and executing the early clinical drug development phase with a project team from researchers, biomarkers, biostatistics, modeling and simulation, toxicology, technical experts and the clinical trial teams. Translational Medicine Experts with an interest in profiling will often continue as members of late stage global project team to characterize the clinical pharmacology, the mode of action, the biomarker response of a compound, look for new potential indications, contribute to the drug approval process, and profile a new compound further in the market. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicineDivisionNIBRBusiness UnitTranslational MedicineLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

People & Org (HR) Business Partner for Digital Commercial Execution

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID285306BRPosition TitlePeople & Org (HR) Business Partner for Digital Commercial ExecutionApply to Job Job Description Why Novartis Digital 155, the approximate number of countries around the world that Novartis products are available in. Our digital transformation leverages cutting edge technology. We make digital solutions for Patients, Carers, Doctors and Novartis employees that improve lives. Our digital solutions help visually impaired patients navigate around cities, critically ill patients manage their disease treatment and doctors make better clinical decisions. We are developing a world-class commercial engine to power our Oncology and Pharmaceutical businesses. This engine is an industry-leading data and analytics platform that will improve the impact of our sales and marketing teams through higher quality tools and solutions that can be deployed faster and at lower cost. A key element of our enterprise-wide digital transformation, this Digital Commercial Execution (DCE) Team works at the interface of four units: Pharma, Oncology, Digital and Novartis Business Services. Within this team, we are applying the concept of Product Teams and Agile working to rapidly innovate and deliver solutions that meet the needs of our commercial teams in both global and country organizations. This team is customer obsessed and as such measures their performance based on business impact. We are seeking a word-class People and Organization (P&O) generalist with TM and OD expertise to be part of the leadership team driving this large-scale transformation of commercial with data and digital. Do you have experience working in product teams or setting up organizations based on product teams? This job is for you! Position purpose Provides strategic and operational HR support globally to the Digital Commercial Execution team which is accountable to Digital, Oncology, and Pharma. Provide world-leading P&O generalist as well as TM and OD expertise to large scale transformation of commercial with data and digital. As Global People and Organization Business Partner to the DCE team your responsibilities will include: • Defining the P&O strategy and priorities to deliver on the DCE goals leveraging the Novartis-wide P&O strategy • Partnering with the DCE team and business units it serves to develop, implement, and evolve the operating model and ways of working to enable product development and deployment that achieves business KPIs • Partnering with the line to define resourcing needs and develop workforce plan to ensure capabilities needed will be build or bought in order to be available on demand • Partner with P&O in Pharma, Oncology, and NBS to  -develop and implement talent management practices to support fluid access to capabilities while developing and retaining our associates  -evolve the broader operating model and capabilities to evolve business practice to transform commercial operations to benefit from digital solutions Minimum requirements • Higher education, such as a University degree in Social Sciences and/or relevant business education (e.g. business administration). English (fluent) Proven track record that includes HR generalist, OD, and TM experience • Experience working in a complex organization, building relationships and driving engagement • Experience in leading transformations at global scale and across a matrix • Experience working in product teams, agile or related transformations highly preferred • Project leadership • Facilitation, coaching and cross-cultural communication skills • Ability to drive results through influence WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionCORPORATEBusiness UnitGROUP HUMAN RESOURCESLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaHuman ResourcesJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Analytical R&D Team Head, Material Sciences (80-100%)

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID283151BRPosition TitleAnalytical R&D Team Head, Material Sciences (80-100%)Apply to Job Job Description 90! The number of New Molecular Entities currently in clinics awaiting to be transformed into successful high quality innovative medicines and in need of team leaders in charge of teams delivering high quality analytical science from the time these molecules leave the discovery laboratory until the transfer to commercial production. As part of the Analytical Research and Development group, this is a new role waiting for you to put your own stamp on it. The position is located at the Novartis Headquarter site in Basel within the Technical R&D (TRD) department of Global Drug Development. Your responsibilities include but are not limited to: • Lead an Analytical Development Laboratory Team responsible for salt and polymorphism, imaging, powder characterization and other material science related analytical activities supporting multiple development products and consisting of a total of 20 - 25 associates. • Contribute to definition and implementation of the global line function strategy by setting appropriate priorities for the team, with particular emphasis on the above mentioned technical areas. • Ensure state-of-the art execution of analytical development activities for drug substances and drug products including method development, method validation and technology transfer. • Ensure team’s compliance to all relevant standards (e.g. HSE and GMP) by proactively identifying potential scientific, technological and GMP gaps or opportunities, proposing and implementing creative solutions. • Champion a true culture of empowerment and innovation, diversity and inclusion, trust, high performance and continuous improvement mind-set. • Ensure best in class partnership with internal stakeholders as well as external vendors and academic institutions. • Strong contribution to advance science, technology and innovation within our analytical research and development department. Minimum requirements What you’ll bring to the role: • Minimum BS / MS in analytical chemistry with focus on API solid state properties or material sciences with significant experience in industry, PhD in analytical chemistry or equivalent desirable. • Minimum of 5+ years of relevant experience (in API solid state properties or material sciences); successful performance and track record in the role of analytical project leader or line/people manager or leading a key initiative or platform, in TRD or a related industrial area. • Sound knowledge of analytical technologies, desired: knowledge of related quality standards (GMP). • Proven track record of successfully managing interfaces to other internal functions, external partners (e.g. Universities) and in being recognized scientific expert by a community outside Novartis. • Ability to work in and/or lead interdisciplinary and/or cross-cultural teams. Desirable: proven leadership skills as people manager as well as a proven ability to work with teams in China. • Understanding of regulatory expectations and profound scientific knowledge in analytical development. • Fluent in English (oral and in writing), German desired. • Ability to perform in a highly dynamic environment. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Analytical Expert - Project Leader (80-100% )

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID283734BRPosition TitleAnalytical Expert - Project Leader (80-100%*)Apply to Job Job Description 450! The number of Analytical Research & Development (ARD) employees globally. ARD sits within the Global Technical R&D department of Global Drug Development. ARD plays an essential role in the characterization and analysis of Small Molecule Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production. We are looking for a highly motivated, experienced Analytical Expert with a strong background and experience in Early Phase Development to join our team. Your responsibilities will include, but are not limited to: • Lead and manage analytical activities within a global project team (e. g. contribute to the technical development plan, lead the specification setting strategy, method development and validation, stability and release testing. • Design, plan, perform, interpret and report results of scientific experiments for the development and preparation and timely delivery of drug substances (DS) and drug products (DP). • Write analytical source documents (e.g Analytical methods, Specifications, Validation reports, Stability reports) and provide input to CMC documents to support regulatory submission. • Prepare analytical project plans and be accountable to meet quality, timelines and budget for assigned projects. • Manage interactions with internal and external stakeholders, including outsourced activities to CROs. Minimum requirements Minimum requirements : What you’ll bring to the role: • PhD in analytical chemistry or equivalent and a minimum 3 - 5 years’ experience in the pharmaceutical industry in analytical development, preferable in early development for sterile products and oligonucleotides. • Proven leadership experience in managing development projects, ideally in a global matrix environment. • Strong quality focus and experience in a cGMP environment. • Excellent understanding and awareness of regulatory guidelines for analytical development. • Profound knowledge in analytical sciences. WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Director Product and Digital Portfolio Management

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID286715BRPosition TitleDirector Product and Digital Portfolio ManagementApply to Job Job Description 2 million patient-years of data to unlock, 12 digital lighthouses scaling and industry leading partnerships! Welcome to Novartis Data & Digital! The last 24 months have seen tremendous momentum in bringing our data and digital transformation to bear! As we are moving from pilot to scale, we need to also mature our own organization. We are hence hiring a Director Product and Digital Portfolio Management into the Digital Strategy and Operations team in Basel to set up and run portfolio management of the digital portfolio, establish a digital productization framework and work directly with product teams in making them successful. We are on an exciting journey and if you enjoy exploring unchartered territory with highly dynamic team, then this is your opportunity! The team Digital Strategy and Program Operations reports directly to the CDO of Novartis and works with him in developing the overall digital strategy and operating model for Novartis as well as in driving select digital lighthouses and bold moves with cross-organizational and group strategic relevance. As the Director Manager Product and Digital Portfolio management you will be responsible to drive the establishment of productization capabilities across Novartis jointly with the IT organization and directly work with product teams across the organization to ensure they can successfully operate in a product setup. You will also be responsible for setting up and running an effective portfolio management of our digital efforts across the company. You will be expected to work with the senior leadership across our businesses and oper-ating functions to drive and execute these efforts. This is a high visibility and demanding role that offers the opportunity to shape the digital transformation at Novartis with a strong focus on execution. You will be responsible but not limited to: As the Director Product and Digital Portfolio Management you would work directly with the Head of Digital Strategy and Program Operations and have responsibility in the following areas: • Work in an agile way owning and setting the direction and vision on Productization, incl., owning, maintaining, and prioritizing the backlog, working with the team, customers and stakeholders to define the roadmap and set appropriate performance targets • Work with the product teams at Novartis for key initiatives to unblock key challenges and opportunities • Evolve the internal process changes needed based on the customer input, experi-ence and feedback to support productization • Develop the enterprise Productization framework codifying into the playbook • Drive development and implementation of a consistent digital portfolio management approach across Novartis, incl., clear definitions and decision criteria • Drive consolidation, monitoring of the portfolio of digital initiatives and identify challenges and opportunities, incl., working with business, IT and finance • Support Head of Digital Strategy and Program Operations in ad-hoc requests You will be expected to work with the senior leadership across our businesses and oper-ating functions to support the CDO in driving the digital transformation. Minimum requirements • Master or PhD in natural science or engineering - MBA from a top business school preferred • High proficiency in English • High empathy and emotional intelligence • 4+ years experience working in product teams, innovation and/or startups or dig-ital tech • High mental agility and proven track record working under significant ambiguity • Several years experience in digital technologies preferred • Demonstrated product management on 2-3 products Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks. And where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help reimagine medicine.DivisionCORPORATEBusiness UnitDIGITAL OFFICELocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaBD&L & Strategic PlanningJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Head of Software Engineering

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID285047BRPosition TitleHead of Software EngineeringApply to Job Job Description 6,000 people dedicated to discovery - 6 research campuses across the globe. Our research is passionate about discovering innovative new drugs that will change the practice of medicine. Novartis Institutes for BioMedical (NIBR) is the global pharmaceutical research organization of Novartis. We have an open and entrepreneurial culture, encouraging collaboration to make effective therapies As Head of the Software Engineering department (~60 internal employees), you will lead a set of teams who are responsible for ensuring the highest quality in software design, engineering, and architecture. You are a role model of Novartis Values & Behaviors: you care about patients, focus on what matters most, dare to challenge the status quo & experiment, take smart risks and always put your team before self. You are an inspiration to the associates who work with you always engaging others in our shared purpose and connect associates’ work with the shared purpose. You ensure you have the right people on your team who live up to our ethics, Values & Behaviors, leadership and culture expectations. You hold people to account and take action when performance and behaviors are not reaching our aspiration as well as continuously foster a learning culture within your teams. You are a learner, not a knower, and you are genuinely curious and open-minded. You empower and support others, create clear accountability, and you remove obstacles for your team. You spend time mentoring and coaching team members and are always clear, present and focused. You ask for feedback, you make it safe to give you feedback and continuously look for ways to improve yourself. Responsibilities include but are not limited to: •Working with the software engineering leadership team to define + ensure common process, standards and tools around software engineering are established and followed by their teams •Helping the product and software engineering planning and development process run smoothly. •Ensuring an engaged, innovative, and inspiring working environment in the department by motivating, challenging, and coaching employees towards growth. •Participating in personnel management practices regarding recruitment and selection, adequate staffing, performance appraisals, education and training, and management development. Minimum requirements What you will bring to this role: •BS/MS in Computer Science, Informatics or similar, or equivalent practical experience •10 years minimum of hands-on software development experience with a minimum of 5 years in a managerial role, and minimum of 5 years with cloud and SaaS (Software as a Service) based solutions. •Experience managing a large, distributed, multi-level, and multi-cultural software engineering organization and the ability to coordinate teams working on multiple, complex, simultaneous, and interrelated software products •Experience developing, implementing and supporting large-scale, highly scalable, highly available, data-driven software and cloud products in enterprise environments •Proficiency with a broad mix of software engineering frameworks, tools, and technologies including web application development and web services, traditional and NoSQL databases, distributed and cloud computing, data visualization, DevOps tools and processes; Successful practical experience with Agile and Lean methodologies and creating a strong DevOps culture •Strong organizational, problem-solving, and influencing skills and proven track record of outstanding teamwork as well as excellent interpersonal, communication, and presentation skills •Ability to travel 25% Preferred skills: •Passion for innovating with data and digital at scale, applying modern technologies to large and complex problems, and creating measurable business value as well as passionate attention to detail, deep empathy for the end-user, and passion for the user experience •Experience with pharmaceutical R&D and good understanding of scientific applications (but not necessarily science itself) •Proven track record of successfully implementing quantitative, data-driven products in enterprise environments •Working knowledge of German or French a plus WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Global Head Clinical Document Governance & Management

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID279666BRPosition TitleGlobal Head Clinical Document Governance & ManagementApply to Job Job Description 500! That’s the approximate number of studies Novartis runs every year in Global Drug Development and Pharma Global Medical Affairs. As the Global Head will define and implement the global Document Governance and Management (DGM) strategy for business and document administration, electronic and paper trial master file document! •Act as the Globally Named Archivist for Global Drug Development be responsible for all the archival activities for Clinical documents •Ensure compliance with global DGM strategy, implements processes and supports technical implementation according to regulations and guidelines, business objectives and innovation opportunities •Accountable for delivery of DGM services and support globally by engaging with vendor partners on operations, management, performance, quality, cost and governance •Define and execute internal and vendor management strategy for DGM including Performance/Service Level Management, Communications and Change Management, and Governance •Ensure DGM function collaborates with various internal partners •Build and maintain paper and electronic clinical document technical standards meeting internal and external requirements. •Define and lead development of clinical document management processes, archiving solutions and related processes and strategies to follow HA guidelines, Good Clinical Practices and Novartis SOPs. Own related SOPs or delegate ownership •Set priorities, decide work load distribution, forecast demand and drive resource / budget planning to ensure adequate delivery of document management services. Minimum requirements What you’ll bring to the role: •At least Bachelors degree in related scientific discipline (natural, pharmaceutical, medical, archival or information technology). •At least 14 years of significant experience in clinical research / pharmaceutical industry and in leading people, teams and projects •Demonstrated experience handling delivery from vendors, audit program, governance. •Strong experience of the clinical drug development and international drug approval processes and related document requirements. •Good Project Management skills and interpersonal skills WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Director Corporate Strategy

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID280323BRPosition TitleDirector Corporate StrategyApply to Job Job Description 105,000 associates here at Novartis aligned to a single inspirational purpose; to reimagine medicine! Reporting to the CEO, the Corporate Strategy team drive high profile, company-wide strategic initiatives that address the top priorities for the company whilst supporting the five core pillars of our Strategy: Unleash the power of our people; Deliver transformative innovations; Embrace operational excellence; Go big on Data & Digital and Return more to society. While our roles are highly visible and demanding, we have a unique opportunity to shape global healthcare trends and work with senior leaders across our businesses to execute our company’s agenda. Your responsibilities: Your responsibilities include, but are not limited to: • Independently drives strategic business projects for Novartis Group, the CEO and the Executive Committee • Generates strategic insights based on best-in-class analysis, distills outputs and recommendations which enable informed decisions of top-level leaders • Actively contribute to annual strategic planning process • Invests in knowledge / functional spike on behalf of strategy team • Proactively identifies trends and opportunities to shape the CEO and ECN agenda • Provide insight into Health Care Systems as our core customer • Develop network of functional experts and strategy managers across Novartis Minimum requirements What you’ll bring to the role: •MD, PhD or MBA from a top business school preferred •High proficiency in English •Deep knowledge of the Pharma industry •At least 4-5 years of consulting experience at a top tier consultancy (engagement manager or associate principal level) •Extensive project and program management experience in strategic projects •Track record of strong business impact •Capability to lead without formal authority •Excellent analytical skills linked with conceptual thinking capabilities •Strong strategic visioning abilities •Ability to reduce complexity into strategy decision recommendations •Excellent communication skills •Strong team player •Desire to work in an international environment •Cross-cultural experience desirable Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. DivisionCORPORATEBusiness UnitCORPORATE STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis International AGFunctional AreaBD&L & Strategic PlanningJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Senior Advisor - Information Products and Data Sciences

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID284543BRPosition TitleSenior Advisor - Information Products and Data SciencesApply to Job Job Description 6,000 scientists and physicians around the world use our data reimagine medicine and create therapies that save lives. You can multiply the value and impact of these data for Novartis scientists. Our research is focused on discovering innovative new drugs that will change the practice of medicine. Novartis Institutes for BioMedical (NIBR) is the global pharmaceutical research organization of Novartis. We have an open and entrepreneurial culture, encouraging collaboration to make effective therapies. At NIBR, our mission is to discover innovative medicines that treat disease and human health. To do that, our scientists need cutting-edge, state-of-the-art computing systems. With NIBR Informatics (NX), NIBR is making a strategic investment into informatics capabilities and is positioning itself to deliver the systems and services that are critical to the future of drug discovery. The Information Products and Data Sciences (IPDS) group in NX is driven to maximize the impact and value to NIBR of software and data. We deliver powerful, functional, beautiful, and integrated software solutions that create a frictionless user experience. Our organization is here to build and apply excellence in product and data management to further Novartis drug discovery. As the IPDS Senior Advisor, you will assist the head of IPDS to develop and run a world-class product organization, create and evolve the IPDS strategy, and guide the organization through its transition to an Agile product team operating model. You will build partnerships with senior business stakeholders, division leadership, and corporate digital leadership to identify opportunities to advance drug discovery. You will interact regularly with colleagues in peer data science and informatics organizations within and outside of the company and will represent the interests of IPDS in NIBR and Novartis initiatives. You may also initiate and coordinate internal IPDS initiatives. Minimum requirements What you will bring to the role: •PhD in chemistry, biology, or other area of science related to drug discovery •Minimum10 years of experience conducting scientific or drug discovery research •5+ years engaged in informatics research or scientific software development •Knowledge of the drug discovery process and pharmaceutical industry Additional required core skills: •Outstanding interpersonal and communication skills; adept at working with colleagues from diverse disciplines and at all levels of the company. •Demonstrated strength as a team player •Strategic thinker •Curiosity about people, organizations, processes, and data •Self-motivated •Strong enterprise mindset and drive to develop collaborative relationships across the organization that multiply your impact •Ability to travel 25% Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine.DivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInformation TechnologyJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Trial Management Development Unit Head

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID283797BRPosition TitleTrial Management Development Unit HeadApply to Job Job Description As our Trial Management Development Unit Head you will lead the Trial Management franchise organization to ensure strategic planning, execution, and delivery of all global clinical trials across all programs within the assigned franchise. You will complete oversight of budget and resource allocation within franchise – including enterprise review of resources across franchises. You will be single point of contact for assigned franchise and act as GDO representative on the Development Franchise Leadership Team. Further, you will drive operational excellence through process improvement and knowledge sharing across Trial Management function. You will develop an empowered organization, which can navigate in a matrix environment and adjust quickly to business needs. Your responsibilities will include: • Drive efficient allocation and resourcing to franchise priorities within broader Trial Management landscape in collaboration with Global Trial Program Heads • Oversight and management of clinical trial budget at franchise level. Core member of the committee responsible for the review and approval of trial budget for assigned franchise • Contribute to shaping the Franchise strategy and translate the Franchise strategy into an operational risk management plan by identifying and appropriately escalating trial and program risk • Drive the mindset of Science of Operations not only in own franchise but as role model and senior leader of the Trial Management leadership team • Serve as single point of contact and trial management representative for assigned franchise for internal/external customers • Proactively identify process improvement and drive excellence in trial operations and management through process improvement in collaboration with other Franchise Heads and Global Head Trial Management • Build best talent and an empowered culture within franchise to foster high performance in a matrix environment. Assess needs of the Trial Management organization to improve the medical/scientific, operational and budget management capabilities in assigned franchise, in alignment with the Global Head Trial Management and other Franchise Heads • Sponsor key talents across the organization to ensure business critical roles and talent continuity for assigned franchise and liaise with other Franchise Heads to secure business continuity across Trial Management Minimum requirements What you’ll bring to the role: • Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD preferred) • Fluent English (oral and written) • ≥15 years of pharmaceutical clinical drug development experience. (with 10 years minimum in global clinical drug development operations) • ≥10 years people management, including leadership of managers and management in a matrix environment. Experience in managing people globally required • Proven leadership and accomplishment in all aspects of conducting global clinical trials and programs • Strong management, interpersonal and problem solving skills • Extensive knowledge of clinical development process, regulatory requirements and Good Clinical Practice (GCP). Novartis experience in these areas is preferred • Proven track record in trial operations process improvement(s) • Considerable organizational awareness, including significant experience in matrix and high pressure environments • Strong knowledge of appropriate therapeutic area preferred WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitGDO GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Senior Scientific Lead, Biologics Pharmaceutical Development (80-100 )

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID285427BRPosition TitleSenior Scientific Lead, Biologics Pharmaceutical Development (80-100*)Apply to Job Job Description >20! That is the number of new biologic entities (NBEs) currently under development in late phase global drug product development. We are seeking an experienced senior professional who will play a key role in the Pharmaceutical Development of complex late stage biologics projects. As senior scientific lead you will shape the design, development and set-up of drug product strategies for parenteral dosage forms of proteins (e.g. monoclonal antibodies, therapeutic proteins, conjugates). You will contribute to scientific governance meetings and the overall Technical Research and Development strategies for NBEs with an emphasis on drug product process development and technical transfer to commercial manufacturing. Your responsibilities: • The successful candidate will act as a senior scientific leader in the Biologics global drug product development organization • You will take on complex late stage NBE pharmaceutical development programs as drug product leader. In this role, you will lead and manage all drug product development activities for the assigned projects within the global drug product development organization, lead and co-ordinate the drug product team (functional experts) and represent Pharmaceutical Development on global CMC teams. • You will lead and manage key scientific initiatives to develop short & long term drug product development strategies for a large NBE pipeline within global drug product development. • You will provide scientific guidance to drug product scientists ensuring scientific excellence within the global drug product and CMC teams. • You will be working in multidisciplinary and international teams, reporting scientific/technical results internally and representing Novartis externally at meetings, giving talks, being part of industry consortiums, publishing papers. Minimum requirements What you’ll bring to the role: • Ph.D. in Chemical Engineering, Biochemical Engineering, Pharmaceutical Sciences, or equivalent 15+ years of successful experience in biotech / pharma industry with emphasis on biologics drug product process development, manufacturing, scale-up, and technology transfer • Experience in protein analytics, lyophilization, primary packaging development for biologics as well as BLA / MAA submission is an advantage. • Proven track record in resolving technical issues as well as in the successful leadership of strategic innovation projects. • Excellent scientific leadership skills, interdisciplinary thinking and proven ability to work in cross-functional, international teams. • Strong presentation skills and scientific/technical writing skills. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Patent Paralegal

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Vollzeitstelle

Back to Previous Page Job ID276802BRPosition TitlePatent ParalegalApply to Job Job Description 30000+ active patent records! That’s the volume we are handling in our global R&D Intellectual Property Operations team. Would you like to join a team that is spread across 5 sites and has members from 7 countries supporting 83 Novartis patent attorneys/agents located around the globe? As part of our team based in Basel, you will support our attorneys to coordinate patent filings and patent prosecution worldwide. Provides a high level of paralegal support including but not limited to filing and prosecution to patent attorneys on the various IP sites (e.g., Basel, US, China and India), ensuring provision of a high quality range of paralegal services to the R&D IP department. To take leadership when assigned in running projects or guiding the work of other Paralegals Core tasks may include but are not limited to the following: • Filing of EP, international and foreign patent applications and related correspondence from filing, issuance of grant and maintenance. • Responsible for meeting patent formalities requirements for EP, US and international patent filings, patent nationalizations into foreign jurisdictions and other conventions. • Responsible for draft preparation of simple responses to official communication and notifications from patent offices/agents. • Independent, proactive and critical review, maintenance and assistance of responsible attorney(s)’ dockets and ensure that all related deadlines are met in a timely manner. • Monitor and update electronic docket for responsible attorney(s) and assigned paralegal tasks on a daily basis to ensure up-to-date dockets. • Coordinate outsourcing, transfer in and transfer out of patent files and responsibilities in a timely and efficient manner, minimizing risk of loss of rights. • Undertake projects to address global prosecution and operational issues affecting department or IP function cross divisionally. • Maintain and share expert knowledge of latest patent rules and adapting practices to comply. • • Be able to mentor or train other paralegals/colleagues. • Role may include patent services data input and invoice processing. • Work to foster a diverse and inclusive environment free from all forms of discrimination and harassment Minimum requirements Paralegal Certificate/IP certification or equivalent experience University/college education preferred 1-2 years exposure working in a global setting, of leading projects and managing its resources a English written & spoken (required) • At least 5 years professional experience as a patent paralegal having worked with or managed resources from law/patent firms • Good written and spoken English 1-2 years exposure working in a global setting, of leading projects and managing its resources. Why consider Novartis? 927 million. That’s how many lives our products touched in 2017. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicineDivisionNIBRBusiness UnitCAO - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaLegal & Intellectual Property & ComplianceJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Global Marketing Director, Dermatology (80-100% )

  • Novartis AG

  • 4040Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID279743BRPosition TitleGlobal Marketing Director, Dermatology (80-100%*)Apply to Job Job Description More than 120m people are affected by psoriasis worldwide, and many others live with skin diseases that significantly affect their quality of life. In our team, we reimagine how our medicines can help improve the lives of patients living with these conditions through our focus on Immunodermatology. Provides leadership to global brand team on the development and execution of marketing strategy for Cosentyx. Works in collaboration with other global functions and country pharma organisations to maximize brand value across all customer groups. Provides effective stakeholder management and leadership. Your responsibilities include: • Leads the development of brand messaging and communication strategies across customer groups • Provides timely input to product development, including new indications and lifecycle management • Leads the development and launch of new initiatives and campaigns including selection and management of multiple agency partners • Provides leadership to design and delivery of marketing mix, balancing ROI with brand KPIs Identifies and shares best practices across the organization • Drives new insights through integration of data from multiple sources, including market research studies, primary/secondary data and competitive intelligence • Integrates insights and data to identify trends, opportunities and threats (worldwide and in key local markets) for product group and proposes corresponding measures • Develops sales forecasts scenarios and sensitivity analyses across a portfolio or brand(s) • Develops pricing options based on market trends and payor insights • In partnership with medical affairs colleagues, creates and leads execution of key expert development program. Contributes to stakeholder mapping • Models strong collaboration and partnership behaviours to ensure optimal effectiveness and delivery Minimum requirements What you’ll bring to the role: • University degree in Science and/or degree in Business, Marketing or Clinical Research • 8+ years’ operational marketing experience with focus on extensive product/brand management including customer facing/sales experience • Immunology / Dermatology therapy area experience with biologic medicines is preferred. • Experience in commercial roles in more than one country and/or prior global commercial experience is preferred. English fluent, additional language is a plus WHY CONSIDER NOVARTIS? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGLOBAL PRODUCT & PORTFOLIO STRATEGYLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaMarketingJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

In vivo Research Scientist, Liver Disease Pharmacology (80-100% )

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Teilzeitstelle 80-100%

Back to Previous Page Job ID286568BRPosition TitleIn vivo Research Scientist, Liver Disease Pharmacology (80-100%*)Apply to Job Job Description 1! Non-alcoholic steatohepatitis is expected to be the number one cause of liver transplant by 2020. We are looking for an agile, curious, and highly motivated Scientific Associate to join in vivo pharmacology team in support of pre-clinical drug development programs for liver diseases. In this role, you will be part of the Discovery and Translational Pharmacology group, in the innovative Disease Area X (DAx) that encompasses a number of therapeutic areas, including hepatology, nephrology, and hematology. Your Responsibilities: • Conduct in vivo and ex vivo experiments on rodents to support preclinical projects and to identify and validate novel targets; the role will involve running established animal models and participation in the development of new models and readouts, performing in vivo efficacy and PK/PD studies, and harvest samples for the evaluation of drug levels, histology, and molecular endpoints. • Perform ex vivo experiments involving molecular, biochemical, and/or immunohistochemistry techniques including developing new ex vivo readouts to support animal models characterization and drug discovery progression. • Work with multidisciplinary team to design studies to assess pharmacodynamics and efficacy of therapeutic candidates in preclinical models. • Learn how to independently plan, execute, document, analyse your experimental results, and draw relevant conclusions, as well as communicate your results in an engaging and thoughtful manner to the project team and broader groups. Minimum requirements What you’ll bring to the role: • M.S. degree in scientific discipline with laboratory-based industrial or academic experience in research • Knowledge and hands-on experience with in vivo research using rodent animal models. Certifications for carrying out animal experiments (LTK Module 1, 2 or a different FELASA Cat. B, C accredited course) is a plus. Knowledge of in vivo drug testing and/or having worked with in vivo procedures in rodents, including multiple routes of dose administration, blood collection, dissection techniques, and tissue collection is an advantage. • Hands-on experience in molecular, biochemical and/or immunohistochemical techniques (Western blotting, ELISA, RT-PCR, histology, IHC) is also desirable. • Excellent oral and written communication skills in English. German desirable. • You are a great teammate, open minded, self-motivated, flexible, and curious to approach new research and disease areas. Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable.DivisionNIBRBusiness UnitCBT - NIBRLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Berufslehre ab 7. August 2020 Kauffrau/Kaufmann EFZ

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Lehrstelle

Back to Previous Page Job ID281132BRPosition TitleBerufslehre ab 7. August 2020: Kauffrau/Kaufmann EFZApply to Job Job Description Kaufleute bearbeiten im kaufmännischen Bereich von Produktions-, Handels- und Dienstleistungsunternehmen sowie in der Verwaltung vielfältige Aufgaben. Selbstständigkeit ist ebenso gefragt wie Zusammenarbeit im Team. Gute Kenntnisse der wirtschaftlichen Grundregeln sowie Gewandtheit im mündlichen und schriftlichen Ausdruck befähigen sie zu vielseitigem Einsatz. Sie arbeiten mit zeitgemässen Mitteln und sind in der Lage, mit der technischen Entwicklung Schritt zu halten. Kaufleute werden ihrer Eignung entsprechend vorwiegend im direkten Kundenkontakt oder in rückwärtigen Diensten eingesetzt. Verständnis für betriebliche Abläufe und Zusammenhänge befähigen sie, im Sinne unternehmerischer Zielsetzungen zu handeln. Minimum requirements Sekundarschule E oder Bezirksschule Organisationstalent, Gewandtheit im mündlichen und schriftlichen Ausdruck, Team- und Kontaktfähigkeit, Freude an Fremdsprachen, Sinn für ZahlenDivisionNBSBusiness UnitHR NBSLocationSchweizSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaPraktikanten / Studenten bei Novartis PayrollJob TypeVollzeitEmployment TypeAusbildung Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

28.01.2020

Novartis AG

Device Development Process Intern

  • Novartis AG

  • 4051Basel

  • 28.01.2020

  • Praktikumsstelle

Back to Previous Page Job ID284212BRPosition TitleDevice Development Process InternApply to Job Job Description 74! The number of medical device projects in Novartis. Without a safe, user friendly, high-quality drug delivery system our patients cannot take their medicine. Device Process Management in Basel needs you to accelerate one of the most diverse and innovative medical device portfolios in the pharma industry. By creating automated solutions for the identification and measurement of key business indicators, you allow us to remove hurdles and enable agile development! You’ll be supporting data analytics and improvement projects within the Technical Research & Development Device organization working within a cross-functional teams. In addition, you will have the opportunity to contribute to the development and improvement of key processes for device development [in compliance with the EU Medical Device Regulations and ISO 13485 as well as US regulations 21 CFR Part 4 and 21 CFR Part 820] as well as contributing to the digital strategy. Your responsibilities: • Creating applications for data extractions. • Analyzing key performance indicators for activities related to medical device development. • Working with stakeholders to identify inefficiencies and obstacles to leaner processes. • Help to create and/or improve procedures and processes to facilitate development of devices for Novartis. Minimum requirements What you’ll bring to the role: • Master Student in Engineering, Biotechnology or Life Science. • Fluent in English (written and spoken), German and French a plus. • Knowledge in statistics • Programming skills in Python, Xml, html, Velocity, Java or similar programming languages. • Medical device knowledge through university studies or direct work experience. • Quick learner, quality focused, good communication and collaboration skills, autonomous and self-driven. Desirable requirements: • Knowledge of regulatory standards for medical devices and/or combination products. • Knowledge in data analytics Please apply with your CV and a cover letter mentioning your availability for this position. Duration: Starting March, for 6 months Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.DivisionGlobal Drug DevelopmentBusiness UnitTECHNICAL R & D GDDLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternship Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

20.02.2020

Novartis AG

Prozessmitarbeiter

  • Novartis AG

  • 9655Stein (Säckingen)

  • 20.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID287692BRPosition TitleProzessmitarbeiterApply to Job Job Description 150! Unser Werk Novartis Stein ist einer der wichtigsten Standorte für innovative, hochqualitative Medikamente, die wir jeden Tag für unsere Patienten in über 150 Ländern produzieren und verpacken. Um die Abteilung Novartis Technical Operations zu verstärken, suchen wir einen Prozessmitarbeiter. Zu Ihren Hauptaufgaben gehören: • Rechtzeitige Bereitstellung und Ablieferung von Einsatzkomponenten für die Verpackung von Medikamenten • Sorgt für Sauberkeit und Ordnung im zu verantwortenden Bereich • Durchführung der Ausserbetriebnahme der Rollenbahn und begleiten der Fremdfirmen • Verwaltung von Verbrauchsmaterialien mit Hilfe Kanban und umsetzen der 5S Standards • Konsequente Einhaltung der SOP`s, Hygiene und Sicherheitsvorschriften Minimum requirements Was ist notwendig für diese Funktion: • Lehre als Logistiker respektive gutes Verständnis für Logistische Abläufe • Vorkenntnisse SAP/Office/MES • Pharma-Erfahrung wie auch GMP Kenntnisse wären von Vorteil • SUVA Staplerausweis, am besten wenn der letzte Kurs nicht länger als 5 Jahre zurückliegt • Fliessende Kenntnisse in Deutsch Warum Novartis? 750 Millionen - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. Wir sind Novartis. Kommen Sie zu uns und denken Sie Medizin mit uns neu.DivisionNovartis Technical OperationsBusiness UnitNTO ASEPTICSLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaTechnical OperationsJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

17.02.2020

Novartis AG

Postdoc / Postgraduate AS&T

  • Novartis AG

  • 4332Stein (Säckingen)

  • 17.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289735BRPosition TitlePostdoc / Postgraduate AS&TApply to Job Job Description 150! Unser Werk Novartis Stein Steriles ist einer der wichtigsten Standorte für innovative, hochqualitative, sterile Medikamente, die wir jeden Tag produzieren und verpacken für unsere Patienten in über 150 Ländern. Um die Qualitätssicherung der Compliance zu verstärken, suchen wir einen talentierten und motivierten Postgraduate / Postdoc ab März 2020 für die Dauer von bis zu 12 Monate. Das Team der AS&T Die Abteilung Analytics, Science & Technology (AS&T) Microbiology ist verantwortlich für die Evaluierung und Validierung von alternativen mikrobiologischen Analysenmethoden für den Bereich der mikrobiologischen Qualitätskontrolle im Rahmen der Herstellung unserer kommerziellen Produkte. In einem dynamischen und herausfordernden GMP-Umfeld bieten wir für talentierte und engagierte Absolventen oder Postdocs ein vielseitiges und flexibles Praktikum/Praxissemester (Zeitpunkt: per sofort). Ihre zukünftigen Aufgaben als Postdoc/Postgraduate – AS&T Specialist • Verantwortlich für die Evaluation, Qualifizierung, Validierung und Einführung neuer mikrobiologischer Testverfahren inkl. automatisierter und schneller Methoden zur Erhöhung der mikrobiellen Qualität und Sterilitätssicherung. • Diese Verantwortung umfasst die Erstellung der entsprechend notwendigen regulatorischen Unterlagen sowie eine regelmässige Berichterstattung über den Projektfortschritt innerhalb des Teams und zu verschiedenen crossfunktionalen Stellen innerhalb der Organisation. • Kontaktperson für analytische Fragen im Rahmen der Evaluation und Validierung von alternativen mikrobiologischen Methoden. • Verfassen und Implementierung von Standard Operating Procedures (SOP’s) für die analytischen Methoden. • Unterstützung des Transfers von analytischen Methoden ins Routinelabor. Minimum requirements Ihre zukünftigen Aufgaben als Postdoc/Postgraduate – AS&T Specialist • Verantwortlich für die Evaluation, Qualifizierung, Validierung und Einführung neuer mikrobiologischer Testverfahren inkl. automatisierter und schneller Methoden zur Erhöhung der mikrobiellen Qualität und Sterilitätssicherung. • Diese Verantwortung umfasst die Erstellung der entsprechend notwendigen regulatorischen Unterlagen sowie eine regelmässige Berichterstattung über den Projektfortschritt innerhalb des Teams und zu verschiedenen crossfunktionalen Stellen innerhalb der Organisation. • Kontaktperson für analytische Fragen im Rahmen der Evaluation und Validierung von alternativen mikrobiologischen Methoden. • Verfassen und Implementierung von Standard Operating Procedures (SOP’s) für die analytischen Methoden. • Unterstützung des Transfers von analytischen Methoden ins Routinelabor. Was wir von Ihnen erwarten • M.Sc. oder PhD in Mikrobiologie, Biotechnology oder angrenzenden Fachbereichen. • Anwendung von Statistikprogrammen wie Minitab, R, Prism. • Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift • Zusätzlich von Vorteil: Erfahrungen im GxP Umfeld, speziell im Bereich der mikrobiologischen Qualitätskontrolle sowie Kenntnis und die Anwendung von entsprechenden Standards für die pharmazeutische Industrie sind von Vorteil • Fachliche Kenntnisse in der Methodik des Next Generation Sequencing (NGS) und der Interpretation der erhaltenen Daten sind von Vorteil. Warum Novartis? 750 Millionen - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. Wir sind Novartis. Kommen Sie zu uns und erfinden Sie Medizin mit uns neu.DivisionNovartis Technical OperationsBusiness UnitNTO QUALITYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

14.02.2020

Novartis AG

QC Professional

  • Novartis AG

  • 9063Stein (Säckingen)

  • 14.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID285014BRPosition TitleQC ProfessionalApply to Job Job Description Novartis Pharma Stein AG ist eines der grössten pharmazeutischen Produktionszentren von Novartis. Es ist unterteilt in die Produktionswerke Solids und Steriles. Unser Werk Stein Steriles ist einer der wichtigsten Standorte für innovative, hochqualitative, sterile Medikamente. Jeden Tag produzieren und verpacken wir tausende Ampullen, Vials, Fertigspritzen und Autoinjektoren für unsere Patienten in über 150 Ländern. Als globales Zentrum für Neueinführungen für sterile Darreichungsformen sind wir kontinuierlich bemüht, unsere Produkte und Mitarbeiter weiterzuentwickeln. Gesucht wird ein QC Lab Professional im Biocenter of Excellence (BoE) Unser Team der Qualitätskontrolle ist innerhalb der Novartis das „Center of Excellence“ für biotechnologisch hergestellte pharmazeutische Produkte. In enger Zusammenarbeit mit den Produktionsbetrieben stellen wir die Qualität und Effizienz dieser Produkte sicher. Neben der Routineanalytik zur Freigabe verschiedenster Medikamente begleiten wir auch Prozessvalidierungen und Markteinführungen neuer Produkte mit unserer Analytik. Wir sind weiterhin für die Durchführung und Auswertung von Stabilitätsanalysen verantwortlich. In einem dynamischen und herausfordernden GMP-Umfeld bieten wir ein vielseitiges und flexibles Aufgabenfeld. Zu den Hauptaufgaben gehören: • Umgang mit einem zukunftsorientierten Biotech Produkte Portfolio und modernster Analyse-Technologien. Im Fokus stehen Bioanalytik mittels HPLC und CE. • Organisation, Durchführung, Auswertung und Dokumentation der chemisch und physikalischen Testung von biotechnologischen Produkten im Rahmen von Freigaben und Stabilitätsstudien für Stein Steriles und weiteren Auftraggebern • Organisation, Durchführung, Auswertung und Dokumentation von Methodenvalidierungen neuer Launch-Produkte sowie laborspezifischer Validierungen • Einhaltung und Überwachung der cGMP-Regeln, SOPs (Standard Operating Procedure) und Sicherheits-Vorschriften • Verantwortlichkeiten für Laborequipment im zugeteilten Bereich • Mithilfe bei Abklärungen von OOS/OOE-Resultaten und Deviations • Mithilfe bei der Vorbereitung von Behörden- und Kundeninspektionen • Aufrechterhaltung schlanker Prozesse und des Informationsflusses innerhalb des Teams Minimum requirements • Abgeschlossene Lehre als Laborant/in oder äquivalente Ausbildung • Erfahrung im Bereich Qualitätskontrolle und/oder Berufserfahrung im GMP/GxP Umfeld • Erfahrung in der Bioanalytik (insbesondere HPLC, CE) • Sehr gutes technisches und analytisches Verständnis • Sicherer Umgang mit MS Office, SAP und Chromeleon von Vorteil • Ausgeprägtes Qualitätsdenken und gewinnende Kommunikationsfähigkeit im Umgang mit verschiedenen internen Ansprechpartnern • Fliessend Deutsch. Englisch Kenntnisse von Vorteil (Wort und Schrift) • Teamplayer, exakte und selbständige Arbeitsweise, detailorientiert • Hohe Eigenverantwortlichkeit und hohe Lernbereitschaft Warum Novartis? 750 Millionen - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. Wir sind Novartis. Kommen Sie zu uns und denken Sie Medizin mit uns neu.DivisionNovartis Technical OperationsBusiness UnitNTO QUALITYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

QA Specialist CGT

  • Novartis AG

  • 9063Stein (Säckingen)

  • 12.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID273386BRPosition TitleQA Specialist CGTApply to Job Job Description 10 days! That is how long we treat a patient’s T-cells, before we return them to potentially save this patient’s live. To support such novel, personalized treatment is a unique challenge within Novartis with immediate patient impact. The QA Specialist CGT is a member of the QA Operations Release Team that is responsible for the final release of product and overall quality oversight of the production and other operational units within Stein C&GT manufacturing. The team ensures that the quality strategy is implemented and that there is a continuous drive to improve product and process quality within the operational units. Your responsibilities: Your responsibilities include, but are not limited to: Support in establishing the SOP landscape relevant for QA Operations, GMP compliant BRR, Apheresis receipt and lot disposition processes during project phase. Independent, flexible processing of all activities related to the release of product during clinical and commercial manufacturing: Technical release of primary packed and finished product, media and apheresis, evaluation and decision of deviations including robust CAPA management, review/approval of batch related quality relevant documents ( e.g. validation documents, transfer documents, APR/PQR), review/ approval of MBRs, review/ approval of executed batch records, audit and inspection support. Minimum requirements What you’ll bring to the role: • Bachelor of Science or Master of Science in Biology, Chemistry, Biochemistry, Microbiology or other related science. • Good understanding of cGMP • Fluent English, German skills desired • 0-5 years of experiences in pharmaceutical QA, QC or production environment; IT-Knowledge (MS Office, SAP, Trackwise, MES) • Ability to communicate clearly with a variety of individuals across different departments in a matrix organizationDivisionNovartis Technical OperationsBusiness UnitNTO QUALITYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkYes Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

Postgraduate im Bereich Sterile Packaging

  • Novartis AG

  • 9655Stein (Säckingen)

  • 12.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289050BRPosition TitlePostgraduate im Bereich Sterile PackagingApply to Job Job Description 80Millionen! Das ist die Anzahl der sterilen Produkte, die in unserem Arbeitsplatz pro Jahr verarbeitet werden. Als Teil des Teams für die Produktion spielen Sie eine Schlüsselrolle bei der Herstellung und Sicherstellung der höchsten Produktqualität für Millionen von Patienten. Unser Werk Stein Steriles ist einer der wichtigsten Standorte für innovative, hochqualitative sterile Arzneimittel. Jeden Tag produzieren und verpacken wir tausende Ampullen und Vials mit hochpotenten Wirkstoffen. Dazu assemblieren wir Fertigspritzen in Safety Devices und Autoinjektoren um unseren Patienten in über 150 Ländern eine benutzerfreundliche und sichere Anwendung unserer Medikamente zu ermöglichen. Als Teil des Teams für die Produktion spielen Sie eine Schlüsselrolle bei der Herstellung und Sicherstellung der höchsten Produktqualität für Millionen von Patienten in mehr als 150 Ländern auf der ganzen Welt. Als Postgraduate im Team der Prozess-Experten in der sekundär Verpackung sorgen Sie dafür, dass in den lokalen pharmazeutischen Produktionsprozessen alle kritischen Prozessparameter und Qualitätsattribute dauerhaft den gesetzlichen Anforderungen entsprechen. Gemeinsam mit den Prozessexperten unterstützen Sie den Produktionsprozess bei GMP/Qualitätsrelevanten Fragestellungen mit Fokus auf Prozessmonitoring, Abweichungsmanagement und Prozessoptimierung im Sinne eines kontinuierlichen Verbesserungsprozesses. Sie analysieren die Leistungsfähigkeit der lokalen Prozesse und initiieren im Falle von Prozessabweichungen oder Trends Abklärungen und gegebenenfalls Verbesserungsprojekte. Wir suchen ab sofort einen motivierten und engagierten Postgraduate für 12 Monate der einen Einblick in die Rolle des Prozessexperten in der sterilen Produktion erhalten und uns aktiv unterstützen möchte. Aufgaben • Bearbeitung von Prozessabweichungen und Beanstandungen aus den Märkten inkl. Root Cause Investigation, Risk Assessment und Definition von CAPA`s • Abarbeitung eigener Projekte im Sinne der Prozessoptimierung • Erkennung von systematischen Performance/Qualitätsmängeln und rechtzeitige Einleitung von Korrekturmassnahmen • Unterstützung bei Inspektionen und Audits • Unterstützung des Bereichs im operativen Tagesgeschäft und bei der Implementierung neuer Technologien Minimum requirements Mindestanforderungen • Naturwissenschaftliches oder Pharmazeutisches Studium • Gute Englisch- und Deutschkenntnisse • Sie sind für ein Studium (Bachelor/Master) eingeschrieben oder haben dieses gerade (vor maximal 12 Monaten) abgeschlossen • Teamfähigkeit und Flexibilität • Offene Kommunikation und Engagement Warum Novartis? 750 Millionen - so viele Menschen erreichen wir mit unseren Produkten . Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. Wir sind Novartis. Kommen Sie zu uns und erfinden Sie Medizin mit uns neu.DivisionNovartis Technical OperationsBusiness UnitNTO ASEPTICSLocationSchweizSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaPraktikanten / Studenten bei Novartis PayrollJob TypeVollzeitEmployment TypeAusbildungShift WorkNein Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

12.02.2020

Novartis AG

2 QC Professionals

  • Novartis AG

  • 9655Stein (Säckingen)

  • 12.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID289227BRPosition Title2 QC ProfessionalsApply to Job Job Description 150! Unser Werk Novartis Stein Steriles ist einer der wichtigsten Standorte für innovative, hochqualitative, sterile Medikamente, die wir jeden Tag für unsere Patienten in über 150 Ländern produzieren und verpacken. Um die Abteilung Novartis Technical Operations zu verstärken, suchen wir zwei QC Professionals. NTO Aseptics offeriert 2 temporäre Einsätze von je 12 Monaten. Während dieser Zeit werden Sie für folgende Tätigkeiten zuständig sein: Aufgaben: • Selbstständige und termingerechte Durchführung von Analysen im Biotech-Bereich nach Vorschriften / Monographien • Protokollieren der Analysenergebnisse unter Einhaltung der damit verbundenen GMP-Richtlinien • Kontrolle der Rohdaten, Eingabe der Resultate ins SAP und Erstellen von Analysenbefunden • Sicherstellen der ordnungsgemässen und zeitgerechten Kalibrierung der analytischen Instrumente und Anlagen innerhalb des Verantwortungsbereichs Minimum requirements Mindestanforderungen • Abgeschlossene Lehre als Chemielaborant/in oder gleichwertige Ausbildung • Gute Sprachkenntnisse in Deutsch und Englisch • Erfahrung im Bedienen von HPLC-Geräten wünschenswert Warum Novartis? 750 Millionen - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. Wir sind Novartis. Kommen Sie zu uns und denken Sie Medizin mit uns neu.DivisionNovartis Technical OperationsBusiness UnitNTO QUALITYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeTemporaryShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Process Expert CGT (Cell & Gene Therapy)

  • Novartis AG

  • 9655Stein (Säckingen)

  • 10.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID279760BRPosition TitleProcess Expert CGT (Cell & Gene Therapy)Apply to Job Job Description You are applying to be part of the Novartis Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV. 10 days! That is how long we treat patient’s T-cells in our production process, before we return them to the patient to hopefully save his live. To support such novel, personalized treatment is a unique challenge within Novartis with direct patient impact. Your responsibilities: Your responsibilities include, but are not limited to: The Process Expert (PE) Supports the Production Unit (PU) in providing front line expert support for all process-specific issues to production: •Provide front line support to manufacturing, working with the shift teams, focusing on manufacturing each batch safely, on time, in compliance with the batch instructions and quality requirements •Responsible for maintaining relevant documents of assigned products (e.g. MBR – Master Batch record, SOP – Standard Operation Procedure) •Act as Subject Matter Expert (SME) for the product and process knowledge •Perform first line evaluation of product and process related issues (deviations, complaints, OOS, OOE – out of specification, out of expectation) •Support process optimization establishment and new technology introduction for continued productivity improvement, as appropriate •Support the execution of process validations, and short-term improvement projects, liaising with all the relevant parties at shop floor to ensure accurate execution •Maintain processes at inspection readiness level and to provide the necessary support in any internal or external audit Minimum requirements What you’ll bring to the role: •BSc. in Engineering, Pharmaceutical Technology, Chemistry, Pharmacy or equivalent scientific degree, Desirable: MSc. or equivalent scientific degree •Fluent in German & good understanding of English •Ability to work in different shifts (also weekend) •Ability to cooperate with other groups / Teams / Departments • Desirable: previous experience in process support role on the shop floor of GMP (Good Manufacturing Practices) manufacturing and/or QA/QC (Quality Assurance / Quality Control). •Proven process understanding (Pharma, GMP, Regulatory aspects) Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. We are Novartis. Join us and help us reimagine medicine. DivisionNovartis Technical OperationsBusiness UnitNTO CELL & GENE THERAPYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaTechnical OperationsJob TypeFull TimeEmployment TypeRegular Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Praktikum im Bereich Automation Engineering

  • Novartis AG

  • 9655Stein (Säckingen)

  • 10.02.2020

  • Praktikumsstelle

Back to Previous Page Job ID288690BRPosition TitlePraktikum im Bereich Automation EngineeringApply to Job Job Description 1957! Seit nunmehr 62 Jahren werden in Stein Medikamente produziert, kontrolliert, verpackt und weltweit versandt – pro Jahr aktuell rund 2 Milliarden Tabletten, Kapseln, Ampullen, Fertigspritzen, Vials und Autoinjektoren. Novartis Pharma Stein AG ist eines der bedeutendsten pharmazeutischen Produktionswerke von Novartis - werden Sie Teil davon - wir suchen derzeit einen Praktikant/In im Bereich Automation Engineering. Im Rahmen eines Praktikums (ab sofort für mind. 6 Monate) ergeben sich sehr vielfältige Optionen zur Mitarbeit, wodurch man einen sehr guten Einblick in die Automation innerhalb des Engineerings eines Pharma-Standortes bekommt. Schwerpunkt des Praktikums liegt im Bereich der OT & Digitalization. Zu Ihren Hauptaufgaben gehören: • Mitarbeit an Automationsprojekten, z.B. im Bereich der vertikalen Integration • Erstellung technischer Konzepte und Spezifikationen • Konfiguration von real-time data management Anwendungen • Harmonisierung der Prozesse (Erstellung und Update von SOPs) Minimum requirements • StudentIn oder AbsolventIn/Bsc/Msc in Automation, Elektro- und Informationstechnik, Informatik, Technische Informatik, Wirtschafts-Ingenieurwesen/IT o.ä. • Hervorragende Deutsch- und gute Englischkenntnisse • Selbständiges Arbeiten und Einsatzbereitschaft • Fähigkeit im Team zu arbeiten • Sehr gute allgemeine Computer-Kenntnisse (besonders Microsoft Word, Excel, SharePoint) • Kenntnisse im Bereich OsiPI Historian Anwendungen und/oder Prozessleitsystemen von VorteilDivisionNovartis Technical OperationsBusiness UnitNTO SITE DEVELOPMENTLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

QA Specialist, Cell & Gene Therapies (CGT)

  • Novartis AG

  • 9063Stein (Säckingen)

  • 10.02.2020

  • Vollzeitstelle

Back to Previous Page Job ID273400BRPosition TitleQA Specialist, Cell & Gene Therapies (CGT)Apply to Job Job Description You are applying to be part of the Novartis Talent Pool. We are currently not recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV. 10 days! That is how long we treat a patient’s T-cells, before we return them in order to potentially save this patient’s live. To support such novel, personalized treatment by ensuring application of correct artwork, is a unique challenge within Novartis with immediate patient impact. The QA Specialist is a member of the QA Analytics & Aseptics Team in QA Operations that is responsible for the final overall quality oversight of the production, Quality Control and other operational units within Stein C & GT manufacturing. The QA Operations team ensures that the quality strategy is implemented and that there is a continuous drive to improve product and process quality within the operational units. Your responsibilities: Your responsibilities include, but are not limited to: • QA Oversight of CGT Quality Control (QC) Unit. This includes QA for release analytics of media and finished product, e.g. FACS, qPCR, ELISA, beads and virus analytics. • QA Oversight of CGT Manufacturing Unit/shopfloor with regard to aseptic topics, e.g. hygiene, aseptic working technique, environmental monitoring, best practice in clean rooms. • Writing, review and/or approval of validation and qualification documents (plans and reports), Out of Specification records, Deviations and other Quality Events, Change Requests, SOPs, risk assessments, testing monographs, transfer documents, lab protocols, trending reports, annual reports, stability reports, certificate of analysis (CoA). • Be point of contact regarding QA questions in quality control and aseptic questions in manufacturing unit, provide ad hoc decisions and act as trainer and advisor on aforementioned topics. • Participate and key person in health authority and internal inspections. Minimum requirements What you’ll bring to the role: • 2-5 years of GMP/GxP experience in pharmaceutical QC, QA, MS&T or production environment, preferably in sterile manufacturing or Cell & Gene (ATMPs) • Strong knowledge and expertise in Quality Control and Aseptics • Strong written and verbal communication skills, ability to communicate clearly with a variety of individuals in various aspects of Novartis operations (QA, QC, PU, MS&T, Logistics) • IT-Knowledge (MS Office, SAP, Outlook, Trackwise, LIMS) Desirable requirements: • BA or MS in Cell/Molecular Biology, Genetics, Biochemistry, Microbiology or related discipline • Fluent in German, good working knowledge in English Why consider Novartis? 750 million. That’s how many lives our products touch. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.We are Novartis. Join us and help us reimagine medicine.DivisionNovartis Technical OperationsBusiness UnitNTO QUALITYLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaQualityJob TypeFull TimeEmployment TypeRegularShift WorkYes Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen

10.02.2020

Novartis AG

Pharmazie-Praktikum im Bereich Verpackung

  • Novartis AG

  • 4332Stein (Säckingen)

  • 10.02.2020

  • Praktikumsstelle

Back to Previous Page Job ID288718BRPosition TitlePharmazie-Praktikum im Bereich VerpackungApply to Job Job Description 1957! Seit nunmehr 62 Jahren werden in Stein Medikamente produziert, kontrolliert, verpackt und weltweit versandt – pro Jahr aktuell rund 2 Milliarden Tabletten, Kapseln, Ampullen, Fertigspritzen, Vials und Autoinjektoren. Novartis Pharma Stein AG ist eines der bedeutendsten pharmazeutischen Produktionswerke von Novartis - werden Sie Teil davon - wir suchen derzeit einen PraktikantIn im Bereich Verpackung von festen Darreichungsformen. Die Process Unit Oral Solid Dosage Forms (PU OSD) setzt sich aus den Bereichen Onkologie, Transplantation, Kardiologie und Diabetes zusammen. Hierbei werden feste Arzneiformen in der Galenik hergestellt und in der Verpackung primär und sekundär verpackt. Ein Teil der Produktionsherstellung der PU OSD sind Lifesaver Arzneimittel. Für talentierte StudentInnen oder AbsolventInnen bieten wir im Rahmen eines spannenden und herausfordernden Praktikums (ab sofort für 6 - 10 Monate) die Chance, an einem anwendungsnahen Projekt in der Verpackung der Prozesseinheit in enger Zusammenarbeit mit Fachspezialisten zu arbeiten und eigenständig mitzuwirken. Die Hauptaufgaben sind: •Entwicklung eigenständiger Lösungsansätze zur Prozessimplementierung und -optimierung •Auswerten von Daten und die Dokumentation von Berichten im Rahmen der kontinuierlichen Prozessverifizierung (CPV) •Erstellung und Überarbeitung von Standardarbeitsanweisungen (SOPs) gemäss den Anforderungen der aktuellen GMP-Richtlinien •Unterstützung des Teams bei operativen Aufgaben Minimum requirements •BSc/MSc StudentIn oder AbsolventIn der Fachrichtung Pharmazie, Pharmazeutische Wissenschaften oder Pharmatechnologie •Exzellente Deutsch- und Englischkenntnisse •Interesse an technischen Prozessen •Proaktive, selbstständige und lösungsorientierte Arbeitsweise •Fähigkeit in multidisziplinären Teams in einem internationalen Umfeld zu arbeiten •Innovativ und qualitätsbewusst •Konsequentes Einhalten der Vorschriften (Sicherheit, Hygiene, Prozesse)DivisionNovartis Technical OperationsBusiness UnitNTO SOLIDSLocationSwitzerlandSiteStein (Säckingen)Company/Legal EntityNovartis Pharma AGFunctional AreaInterns/Students on Novartis PayrollJob TypeFull TimeEmployment TypeInternshipShift WorkNo Apply to Job Access Job Account TwitterTweet FacebookShare Share Twitter Facebook LinkedIn Email Whatsapp Jump to Comments Print
Inserat ansehen