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IQVIA AG

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IQVIA AG

Dorfplatz 4
6330Cham

01.04.2020

IQVIA AG

Consultant, Technology Solutions

  • IQVIA AG

  • 4040Basel, CH

  • 01.04.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Your mission: Joining our Team ad as a Consultant within Technology Solutions, you will work with high caliber project teams to deliver short term and long term projects for Life Sciences clients mainly in the domains of Commercial Technology. Your role will encounter the following tasks: Collecting, organizing and analyzing business requirements aligned with clients business strategy Taking part in business process decomposition and re-engineering in technology implementation project teams. Supporting Technology teams in developing technical architecture that meets the client requirement. Supporting other project activities for commercial technology such as UAT, TTT, Gap fit and demos. Supporting project management activities such as weekly calls, project plan maintenance, risk and issue management. Preparing relevant project documents e.g. business requirements documents, training materials etc. Performing client interviews, assisting in interview guide development and summarizing interview notes Enhancing the client’s ability to function effectively and independently by training and developing client teams Acting as Business Analyst and IT integration consultant, creating work artifacts, deliverables and providing reports to clients and internally accordingly Traveling to and working at client sites in various cities and countries as needed. Your profile: Master degree or equivalent in business administration, computer science, engineering or related discipline, or knowledge acquired through equivalent experience. 3 years relevant working experience, ideally acquired in Life science/pharma oriented services/consulting or IT solutions / system integration. Good understanding of commercial customer engagement concepts in pharmaceutical industry. Ability to bridge technology and business requirements from our clients. Proven track record in project work. Strong commitment to effective, cross-functional teamwork. Fluency in English is a must, any other language is of advantage. Role location: Basel Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1107422
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01.04.2020

IQVIA AG

Senior Consultant, Technology Solutions

  • IQVIA AG

  • 4040Basel, CH

  • 01.04.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Your mission: As a Senior Consultant within Technology Solutions, you will work with high caliber project teams to deliver short term and long term projects for Life Sciences clients mainly in the domains of Commercial Technology. Your role will encounter the following tasks: Collecting, organizing and analyzing business requirements aligned with clients business strategy, acting as a trusted adviser and recommending process changes based on industry best practices. Taking a leading role in business process decomposition and re-engineering in technology implementation project teams. Supporting Technology teams in developing technical architecture that meets the client requirement. Support and lead other project activities for Commercial Technology such as UAT, TTT, Gap fit and demos. Supporting project management activities such as weekly calls, project plan maintenance, risk and issue management. Preparing relevant project documents e.g. business requirements documents, training materials etc. Performing client interviews, assisting in interview guide development and summarizing interview notes. Enhancing the client’s ability to function effectively and independently by training and developing client teams. Acting as Business Analyst and IT integration consultant, creating work artifacts, deliverables and providing reports to clients and internally accordingly. Traveling to and working at client sites in various cities and countries as needed. Your profile: Master degree or equivalent in business administration, computer science, engineering or related discipline, or knowledge acquired through equivalent experience. 5 years relevant working experience, ideally acquired in Life science/pharma oriented services/consulting or IT solutions / system integration. Good understanding of commercial customer engagement concepts in pharmaceutical industry. Ability to bridge technology and business requirements from our clients. Proven track record in project work and first experiences in leading (sub) streams in larger client projects. Strong commitment to effective, cross-functional teamwork. Fluency in English is a must, any other language is of advantage. Role location: Basel Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1107423
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31.03.2020

IQVIA AG

Consultant, Technology Solutions BI and Performance Management

  • IQVIA AG

  • 4051Basel, CH

  • 31.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Key Responsibilities: To support us in the growth of our activities, we are looking for a new Team Member who will be given the opportunity to work on BI projects: Run workshops, participate in requirement development & gathering process Translation of client requirements into specification Collaborate with the technical teams spread across geography and translate the requirements Ensure that the client's business need is fully understood by the project team and that the solution will meet the requirements Participate in testing activities   Write documentation (e.g. URS, FS, Test cases) Work collaboratively in a large team Manage small projects, workstream or change requests Support business development activities, contribute in proposal development Essential experience, technical and personal skills: MSc/MA in computer science, engineering or equivalent experience Prior hands-on experience (from 3 to 5 years) in business & data analysis and requirements definition for Information Management or Business Intelligence solutions is necessary Professional expertise in Consulting (Life Sciences and/or Business intelligence domain) Ability to run workshops, participate in requirement development, gathering process and translation of requirements into specification Good understanding of Commercial Analytics in Life Sciences is a plus Experience with data analysis using SQL, Python or similar Manage small projects from the delivery perspective or ambition to grow into it Proficient skills in teamwork, collaboration, excellent communication abilities Experience with business Intelligence (Tableau, QlikView), Data Warehouse, Cubes, ETL is highly beneficial Experience with software life-cycle developments is appreciated Experience with a CRM is of advantage Languages: Fluency in English (oral and written), German or French are a plus Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1115186
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26.03.2020

IQVIA AG

Head of Technology Solutions Switzerland

  • IQVIA AG

  • 4051Basel, CH

  • 26.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. We are looking for a new colleague to join us as Head of Technology Solutions Switzerland . Start date: as soon as possible. Your mission: In this role, you will lead the Swiss IQVIA Technology Solutions sales-, delivery- and service teams and grow the business in Switzerland in close collaboration with Key Account Management and the regional Technology Solutions team. Grow revenue and grow client base across the QI Technology & Applications portfolio (Marketing Automation, CRM, Performance Management and BI solutions, Compliance solutions, custom development, etc): Set sales and operational strategy; plan adequate customer segmentation and detailed offering execution Hands-on sales engagement, leading or co-leading key customer opportunities, preparation of client discussions, meeting with CxO level executives Hands-on coverage of strategic accounts Monitor and manage client retention; mitigate risks to existing customer base Plan and execute respective marketing and promotional activities; in close collaboration with the respective Marketing/MarCom specialists; capture public speaking opportunities Manage the Technology solutions business: P&L responsibility Define goals, establish metrics and performance management culture Ensure a predictable forecasting process and figures; ensuring appropriate pipeline management to achieve objectives Ensure delivery and service excellence through solid planning and staffing (incl. off-shore teams where needed) Optimize the team structure to maximize delivery efficiencies via near- and off-shoring capabilities Leadership of the sales, delivery and service teams Your profile: University degree in business administration, economics, IT, mathematics or economics 10+ years experience in Life science/pharma oriented services/consulting or IT solutions / system integration, including direct sales experience on complex, consultative sales processes 5+ years of management experience (ideally sales management / business development) Relevant expertise in client delivery, project management Profound knowledge of the pharma industry and its core commercial processes (possibly acquired first hand in an industry role) in particular sales and (multichannel-) marketing Seniority and gravitas to engage credibly at C-Suite level in Life Science HQs, supported by a profound knowledge of key Life Science / Pharma business areas like R&D, Pricing & Market Access, Sales & Marketing Highly proactive entrepreneurial attitude, objective oriented and self – driven / self starter, capable to drive the business without major guidance Strong hands-on consultative selling approach (analytical, structured thinking; issue-based conversation style; creative solution sales approach) and an ambition for innovation Strong networker at client and internally; Ability to work collaboratively, capable of pulling the right expert teams together and coordinating them to create top-notch solutions Excellent presentation, communication and influencing skills (including public speaking) and capable of communication the total IQVIA value proposition to a broad range of senior client stakeholders Fluency / Mother tongue in English is a must; German is a plus Home base in Basel, Zurich or central Switzerland region Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1102020
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26.03.2020

IQVIA AG

(Senior) Principal - Technology Solutions

  • IQVIA AG

  • 4040Basel, CH

  • 26.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. We are now looking for new colleagues to expand our growing Team. Start date: as soon as possible. Your mission: As a (Senior) Principal within Technology Solutions , you will work directly with clients to develop business opportunities and deliver projects ensuring that delivery results are at high levels of client satisfaction. Your missions will encounter the following: Identifies, develop and elevates business opportunities and potential growth areas for our technology solutions business. Owns client accounts and drives the BD activities to the account incl orchestration of multi-disciplinary teams. Maintains in-depth and extremely current knowledge of client/business strategies, business issues and relationships. Act as principal owner of client engagements; ultimate responsibility for client satisfaction and delivering high levels of quality/added value. Develops awareness of technology solutions and how they can be utilized in client scenarios. Uses technical skills to provide objective advice and expertise and help organizations develop or implement technical strategies to optimize performance. Remains up to date with current trends in technology services and provides direction to anticipate and identify business challenges and issues. Has responsibility for people management and talent development to meet business growth and changing priorities. Coaches/mentors teams and contributes to driving technical thought leadership. Your profile: Master’s degree in business administration, economics, IT, mathematics or economics or equivalent. 10+ years experience in Life science/pharma oriented services/consulting or IT solutions / system integration, including direct sales experience on complex, consultative sales processes. Experience in a Senior Management or Senior Sales / KAM position, with proven ability as a leader. Experience leading cross functional and geographically spread teams in delivering commercial technology services projects of significant size and scope. Proven business development skills. Strong client relationship up to C-Suite level executives, strong networking and influencing skills. Able to manage complex relationships and juggle priorities. Broad knowledge of the Pharma and Life Sciences industry. Can-do and positive attitude, strong influencing skills. Ideally possesses in-depth understanding of IQVIA data assets and IQVIA core offerings. Demonstrated strategic thinking and planning and change management skills. Role location: Basel. Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1102014
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26.03.2020

IQVIA AG

Business Development Director (France OR Switzerland)

  • IQVIA AG

  • 4051Basel, CH

  • 26.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. The role will be responsible for selling the entire solution portfolio across R&D. Candidates will need to bring past solution selling expertise with a track record of leveraging organizational capabilities in order to upsell, driving a more sophisticated and integrated sales approach helping to shift the market to the benefit of the company. We believe in hiring the best sales talent in the life sciences industry and candidates should possess strong intellect and analytical skills. Critical will be the ability and agility to survive and indeed, thrive, with ambiguity and complexity. Given that IQVIA is charting a new path there will be a need to work collaboratively across the organization and so a sophisticated approach to relationship building, both internal and external, will also be essential. In light of the above, candidates for the roles should exhibit the following skills and competencies: A high level of drive and resilience reflected in a track record of sales and business development success in past roles. • A passion and strong understanding of the life sciences market Biopharma or Medical Device Research and development experience is beneficial but not essential. Our best-in-class training will provide the best life sciences sales professionals with the skills and information they require to sell IQVIA’s offerings Excellent communication skills and so able to communicate the total IQVIA value proposition to a broad range of client stakeholders. Ability to lead and manage bid teams without direct line reporting. Ability to lead and manage complex negotiations. Demonstrable track record of building strong strategic and trusted relationships with client stakeholders. Ability to navigate ambiguity and have the self-awareness to know when to bring in the appropriate SMEs across a complex portfolio of expertise • Clear business acumen and creative problem-solving aptitude Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1101989
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26.03.2020

IQVIA AG

IQVIA CSMS Schweiz sucht Pharmaberater (m/w)

  • IQVIA AG

  • 4051Basel, CH

  • 26.03.2020

  • Vollzeitstelle

Job Description Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. Ihre Aufgabe Sie besuchen mit Fach- und Sozialkompetenz niedergelassene Ärzte, Spitäler und Apotheken in der ganzen Schweiz. Dank Ihrer Verkaufserfahrung wissen Sie, wie Sie Ihre Gesprächspartner auf ganzer Linie überzeugen können. Sie sind eine analytisch denkende Persönlichkeit und können sich gut organisieren aber auch Teamspirit ist kein Fremdwort für Sie. Sie erkennen sich wieder? Dann lesen Sie weiter. Ihr Profil Sie sind eine selbständige und empathische Verkäuferpersönlichkeit mit guten Kontakten im Schweizer Pharmamarkt Sie verfügen über eine naturwissenschaftliche oder paramedizinische Ausbildung/Studium oder haben ein SHQA Diplom und bringen Erfahrung im Pharmaaussendienst in verschiedenen Indikationsgebieten mit Sie beherrschen die deutsche Sprache sowohl mündlich wie schriftlich und haben gute Französisch und/oder Englisch Kenntnisse Sind Sie bereit sich neuen Herausforderungen zu stellen? Dann bewerben Sie sich mit Ihren vollständigen Unterlagen. We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™ Job ID: R1076746
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23.03.2020

IQVIA AG

Paralegal or (Junior) Regulatory & Study Start-Up Specialist (m/w/d) - office based in Basel

  • IQVIA AG

  • 4040Basel, CH

  • 23.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. We currently have an exciting opportunity as Paralegal/Legal Assistant, Contracts or (Junior-) Regulatory & Start-Up Specialist (m/w/d) to work in both fields of ethics and submissions and contracting and budget negotiations in our Regulatory & Start-up Department in  Basel. Alternatively you can be based in Freiburg i.Br. , Germany or Vienna , Austria. You will support the initiation process of clinical research trials by arranging investigator contracts with study sites like hospitals and medical doctors’ offices and perform tasks associated with Start-up and Maintenance activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. While projects vary, your typical responsibilities might include:   Review, prepare and negotiate site contracts and budgets with sites. Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information. Ensure contracts are fully executed, regulatory documents and approvals are granted, IP Release authorized and specific project deliverables are completed. Review, establish and agree on project planning and project timelines. Ensure overall project efficiency and adherence to project timelines. Ensure monitoring measures are in place and implement contingency plan as needed. May provide input into contract and budget template development. May act as Local Contract Expert. May act as mentor, and prepare and deliver country-specific training, for less experienced staff. You should have: Apprenticeship or Bachelor’s Degree in the field of law or economics and at least 2-3 years of contracting experience, preferable in the life science sector  Alternatively a Bachelor’s or higher level degree in life science or similar scientific discipline and clinical trials experience Effective communication, organizational and planning skills Fluent languages skills in German and good command of English; French or Italian is a benefit Ability to work independently and to effectively prioritize tasks Ability to work on multiple projects Ability to establish and maintain effective working relationships with coworkers, managers and clients Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1098212
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23.03.2020

IQVIA AG

Clinical Risk Manager- Sponsor Dedicated (Novartis)

  • IQVIA AG

  • 4040Basel, CH

  • 23.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Clinical Risk Manager - Novartis dedicated The Clinical Risk Manager supports the pro-active and continuous improvement of quality, data integrity and general regulatory / ICH-GCP requirements across Global Development Operations (GDO). The Clinical Risk Manager is responsible to support the identification and mitigation of relevant cross-functional, systemic risk and issue trends as well as track high-level the status of the investigation and remediation progress of high-impact, functional, systemic risk and issue trends. He/she is responsible to analyze available data sources for cross-functional, systemic issue and risk trends and to perform data-driven and thorough root cause analyses followed by tracking subsequent remediation activities (workstreams, initiatives, etc). Major Accountabilities:   Contributes to the development and maintenance of a standard business process across GDO that aims at triaging and reporting of systemic quality issues and risks to the appropriate escalation and decision level. Contributes to the development and maintenance of an appropriate issue and risk registry for systemic quality risk and issue trends across GDO. Analyzes available data sources on potential, GDO-relevant, cross-functional, systemic quality risk and issue trends and performs a risk assessment considering at minimum frequency/likelihood of repeat occurrences and degree of impact. Brings results forward to GDO QRB to agree on route of action. Where the need for remediation is confirmed by GDO QRB, performs a data-driven root cause analysis to identify which areas in particular need to be improved to avoid repetition of cross-functional, systemic quality issues moving forward. Upon identification of key root causes of cross-functional, systemic risks and issues, contributes to cross-functional teams in identifying, planning and implementing appropriate mitigation plans. Ensures that improvements are measurable and that effectiveness checks will be in place. Aligns with the process excellence groups across GDO and beyond (e.g. GDD, NIBR, GMA) to ensure that any function-specific risk and issue trends that were incidentally identified while reviewing and scouting data have been or will be picked up by the respective functional group for further analysis and mitigation. Tracks progress of mitigation plans and their implementation for cross-functional risks as well as high-impact functional risks. Tracks whether improvement targets are met and where not raises it for further action. Contributes to the development / enhancement of GDO-wide key risk / quality. Contributes to the development of feedback loops with GDO associates on identified systemic issues, risks and planned mitigations to enable them to plan these in to their own project plans. May contribute to workstreams and initiatives across Novartis. Key Performance Indicators (Indicate how performance for this role will be measured) Results from trend and root cause analysis available in a timely and data-driven manner Mitigation plans are targeted and have measurable effectiveness checks included which are either being met or mitigation plans adjusted until desired targets are met Key Quality Indicators show an upward trend over time. Experience/Professional requirement: Minimum Bachelor’s degree in life science, quantitative science or business or equivalent Fluent English (oral and written) 3 - 5 years of experience in clinical operations 1 -2 years of experience in a risk management, quality management, process improvement or related role Good understanding of the drug development process and ICH-GCP requirements Experience with data mining/analysis, basic statistical methodologies as well as root cause analyses Ability to think independently and out of the box and able to assess complex problems Good project management skills Proven networking skills and ability to share knowledge and experience amongst colleagues. Proven ability to work in a complex matrix environment (including remote or virtual team environment). Organizational awareness, including experience working cross-functionally and in global teams. Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1124158
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21.03.2020

IQVIA AG

Associate CRA / CRA / Senior CRA (f/m/d) - office-based in Basel or St. Prex or home-based in Switzerland

  • IQVIA AG

  • 4040Basel, CH

  • 21.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. We are currently hiring an Associate CRA, CRA or Senior CRA (m/w/d) to work in our sponsor dedicated department and to join  office-based in Basel or St. Prex or home-based in Switzerland .   While projects vary, your typical responsibilities might include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You should have: A Bachelor's degree in a health care or other scientific discipline or educational equivalent At least one year of on-site monitoring experience Alternatively, you should have an equivalent combination of education, training and experience Excellent communication skills in English language including good command of  two of the following languages:  German ,  Italian or French You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. Flexibility to travel If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team .  Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1055386
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15.03.2020

IQVIA AG

TMF Domain Expert- Sponsor dedicated

  • IQVIA AG

  • 4051Basel, CH

  • 15.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. TMF Domain Expert - Novartis dedicated Senior Domain Expert for Trial Master File (TMF) documents to support Source-to-Target Migrations of Clinical Documents. This resource will lead Migration Data Preparation activities and assist to determine all properties and attributes for all types of TMF documents.  Major Accountabilities:   Collaborate with external vendor and NVS internal functions to: Build, expand and automate the migration approach for TMF documents from Source to Target System Build, expand and automate the Attribute Extraction Approach to determine mandatory document properties Coordinate & oversee processes supporting extraction and migration activities by: Driving Quality Control activities to ensure that the migration / migration automation process is producing high quality outputs Coordinating and participating in Test Activities Ensuring appropriate completeness checks for the Trial Master File (TMF) records of migrated clinical studies Collaborate closely with CDGM organisation and business process owners to ensure alignment of migration activities with parallel system and/or process updates. Engage with stakeholders in the Novartis organization to align on migration requirements, migration approach and missing or erroneous information in source system Support Novartis Digital ambitions and gain insights on Artificial Intelligence projects The above responsibilities are to a large extent based on interdisciplinary topics and require the employee to liaise, cooperate with and coordinate numerous related functions such as users from different business areas, CDGM functions, IT, QA, etc. Key Performance Indicators (Indicate how performance for this role will be measured) Consistency, Compliance and Integrity enabled for TMF Migration Processes Adherence to Novartis Standards and Stakeholders Expectations on TMF Migrations Experience/Professional requirement: Minimum Bachelor’s degree in life science/healthcare or equivalent Fluent English (oral and written), German of advantage   Minimum 10+ years experience in LifeScience Industry Extensive experience with usage of clinical document management systems Working knowledge of clinical essential documents, including Trial Master File (TMF) Relevant clinical research experience in industry or in clinical practice such as  trial/study coordinator Experience with coordinating deliverables from 3rd party vendors Knowledge of ICH GCP, 21 CFR part11 Experience with Documentum based D2LS system is a plus. Experience with Document Migration Projects is a plus Experience working as Business Analyst is a plus Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1123207
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15.03.2020

IQVIA AG

Clinical Document Processing Manager- Sponsor Dedicated

  • IQVIA AG

  • 4051Basel, CH

  • 15.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Clinical Document Processing Manager - Novartis dedicated Ensure efficient and appropriate management of the Clinical Document Processing activities and processes, as well as the Processing team. Coordinate the In-Licensing / Out-Licensing / Divestment Projects and ensure successful transition of TMF doc-umentation within/outside of Novartis. Major Activities:   Ensure high quality and efficiency of Clinical Document Processing standards in accordance with HA Guidelines, Good Clinical Practices, Novartis SOP’s: Support the Clinical Document Processing & Archiving Lead to define the strategy for the Processing activities Manage and coordinate the Processing services/activities and team (provided by external partner), including prioritization of projects, team assignments,: Manage and globally coordinate the creation and/or update of applicable processes, Guidance documents, templates, etc... as applicable Support with the budget planning/ forecast to ensure adequate delivery of processing services by the dedicated ESP Ensure business support for high quality, timely and efficient processing of paper and electronic documents.: Keep oversight over processes and infrastructure for filing, indexing, archiving and retrieving of study documentation and ensure their compliance. Act as an SME for the document processing in the electronic Document Management Systems (CREDI/SubWay), i.e. Artifact / Doctypes, Naming Conventions, Attributes, Properties, etc Ensure quality, inspection-readiness, timeliness and efficiency of facility management and Clinical Documentation handling such as scanning, QC, technical fixes as well as management of exceptional (legacy documents, in-licensing/out-licensing documents) and time-critical documents. Ensure support in the preparation and during audits and inspections. Coordinate and act as primary point of contact for the In-Licensing / Out-Licensing / Acquisition / Divestment Projects: Coordinate the Clinical Documents Governance and Management activities (paper and electronic), Proactively and successfully, collaborate with key stakeholders including the Archiving team, other groups from Clinical Document Governance and Management, Development Informatics, Legal, Development Quality Assurance and Global Project Teams... Lead and/or Contribute to the development of the TMF Transition Plans Ensure successful transitions of TMF (paper and electronic) Support the TMF Manager Outsourced Studies in the different Outsourcing strategies (e.g. direct import by ESP), Outsourcing processes, etc... Develop and maintain paper and electronic document processes & standards in compliance with internal and external requirements & regulations; own related SOPs or delegate ownership; support and/or drive improvements and innovation on business and technical aspects of TMF processing, including implementation of innovative methods. Promote best documentation practices to line functions to ensure that documents created/generated in the course of clinical research are managed and archived in accordance with GCP guidelines and Novartis SOPs Key Performance Indicators (Indicate how performance for this role will be measured) Inspection-readiness of TMF Documentation and processes – no critical audit or inspection findings Timely and high-quality importing and filing of TMF documents (paper and electronic) Consistent and efficient use of Processing / Outsourcing Processes in Line Organizations Definition of quality standards for documents and document processing Experience/Professional requirement: Life science university degree / Bachelor’s degree in life science/healthcare is required with minimum 5 years’ experience in clinical operations and / or clinical systems management Associate degree required with minimum 8 years’ experience in clinical operations and / or clinical systems management Fluent English (oral and written) Experience in monitoring and quality control of deliverables provided by external vendors Knowledge of the technical requirements by FDA/EMA for submission documents Advanced ability to work both independently and in a global cross-functional multicultural and international team.       Ability to lead globally distributed matrixed teams. Demonstrated ability to influence without authority. Demonstrated experience managing delivery from vendors Knowledge of clinical development process and/or document management (paper and/or electronic), regulatory requirements and Good Clinical Practice. Ability to translate trial information, processes and regulations into TMF documentation. Excellent attention to accuracy and details, organization and tracking skills. Good interpersonal, problem-solving, negotiation and conflict resolution skills. Good communication skills Ability to work under pressure Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1123208
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12.03.2020

IQVIA AG

Executive Assistant

  • IQVIA AG

  • 4040Basel, CH

  • 12.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Are you up for a challenging and exciting opportunity? We are looking for an Executive Assistant to join us on a newly created position. S tart date: as soon as possible Your mission: By providing personalized and timely support to Senior Management on a daily basis, you will ultimately contribute to the efficiency and continuity of the business. Your responsibilities will include: Under general supervision and acting on own initiative, performs diverse and advanced secretarial and administrative duties for senior management. Proactively handles complex calendar and logistical arrangements for senior management travel. Is responsible for meetings organization and client events across Europe Including liaison with client teams and business partners. Answers mail and inquiries on own initiative, proactively choosing the appropriate medium. Manage information flow in a timely and accurate manner. Format information for internal and external communication – memos, emails, presentations, reports. Prepares, checks and processes expense reports for several senior executives. Secures and maintains a high service culture and client satisfaction Your profile: High school or equivalent diploma and advanced administrative training with proven prior related experience. Ability to manage multiple stakeholder relationships up to a senior level.  Highly organized with an eye for detail and accuracy. Excellent working knowledge of commonly used Microsoft applications, including Outlook, PowerPoint, Excel and Word. Experience of complex international diary management, travel and accommodation scheduling. Strong communication, organizational skills and discretion essential. Proven experience within a fast-paced organization delivering efficient and reliable administrative and co-ordination support. Enthusiastic proactive team player. Fluent in English and German. P lace of work : Basel Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1117922
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12.03.2020

IQVIA AG

Senior Clinical Research Associate (f/m/d) - office- or home-based in Switzerland

  • IQVIA AG

  • 4040Basel, CH

  • 12.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Create possibilities, even where it seems none exist. See every challenge as an opportunity. Discover new paths to success as you share stories of unparalleled data, transformative technology, advanced analytics and domain expertise coming together to advance human health.  Join IQVIA™ as a Senior CRA (f/m/d), and you will have the opportunity to plan and progress your career in the direction you choose. At IQVIA™ we do not believe in a ‘career ceiling.’ You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Responsibilities include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. We believe in hiring the best clinical talent in the industry. Applicants should have; A Bachelor's or higher-level degree in a health care or other scientific discipline or educational equivalent At least three years of on-site monitoring experience Alternatively, you should have an equivalent combination of education, training and experience Strong written and verbal communication skills including good command of German and English language, additionally French and Italian language skills would be a plus In return we offer: Interesting projects, a variety of indications and different sponsors Working with high-level equipment and technical solutions A competitive benefits package: Home-Office, Generalabodement, and Accident Insurance. If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team .  Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1117947
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07.03.2020

IQVIA AG

Principal Consulting - Real-World Insights

  • IQVIA AG

  • 4051Basel, CH

  • 07.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. In our Real World & Analytics Solutions (RWAS) team, we design and deliver innovative, data– and technology-enabled evidence programs for the pharmaceutical industry. We apply scientific rigor and advanced analytics to real world data to help our clients improve healthcare. This entrepreneurial team works within Switzerland, a global pharmaceutical industry hub, partnering with global colleagues throughout the enterprise to diagnose critical business issues and deliver evidence-based solutions. Real- World & Analytics Solutions, Enterprise Solutions Team We are strategic thinkers, innovative technologists, deep subject matter experts and data evangelists whom are passionate about driving better performance in healthcare. We are collaborative, intellectually curious, entrepreneurial and disruptive. Plus, we have the resource and structure of a large company in an environment where we empower our people to create their own solutions. Our work can be complex and difficult but that is often the case when you are doing work that no one has done before. We also do not have a templated approach to our work so we require people who can innovate with their practice as well as their solutions.  If you have the right levels of intellectual curiosity and a passion to discover the real impact of medicines in the real world, then you’ll fit right in. Role description As a Principal you will be able to develop business and implement innovative data-driven solutions with clients. Innovation is at the very core of RWAS and this role. You will be responsible for engaging headquarters clients to develop custom RWAS, developing innovative product offerings and leveraging latest innovation in technology and data science to develop value added solutions. Principal Accountabilities Strategy setting and market building Take a leadership role in implementing RWAS business vision and objectives and supporting the strategic development of the business Identify new opportunities for innovative data solutions and platforms Identify and frame partnership and other partnership/acquisition opportunities Build and maintain external stakeholder relationships to promote IQVIA market positioning, access to data and relationships with key influencing groups Contribute to the development of the IQVIA thought leadership and innovation agenda Client leadership and project delivery Consult with customers to fully understand their needs, develop high quality proposals to address these needs and lead project delivery Engage senior leaders at key accounts to drive overall RWAS service growth opportunities Lead teams of RWAS professionals in the design, development and delivery of complex RWI products to a high standard which meet or exceed client expectations Engage closely and supervise cross-functional IQVIA teams to ensure the full complement of IQVIA capabilities and solutions reach customers Capabilities building and people leadership Expand capabilities and capacity in patient data assets and networks, healthcare intelligence tools and commercial and scientific services Responsibility for line management, coaching, mentoring and the development of more junior employees as well as participating in recruitment activities  Desired Skills and Experience Leadership experience in Healthcare with focus on data, technology and analytics including working with senior clients Managing teams to deliver client work to high quality and standards Experience in product development, from initial concept development, market sizing through to product delivery plans A track record of driving HQ/global deals, aligned with suitable offerings development experience Proven ability to advance ambiguous or conceptual ideas and engage multiple stakeholders, internal and clients, to decision points A track record of thought leadership, publications and public speaking Offerings development experience – familiarity with accepted innovations models e.g. open innovation, ideation, product platforming, immersion or similar would be beneficial Leadership experience in complex organizations with demonstrated results in aligning people without formal reporting relationships Good understanding of the types of analyses conducted in healthcare databases Overall understanding of different technology domains (infrastructure, architecture, analytics applications) and experience of managing technology programs Word and PowerPoint competent, the ability to develop clear storylines and business cases. Knowledge of consulting methods, tools, techniques Deep commercial awareness of the healthcare, health technology and pharmaceutical industry, gained through experience Understanding of and interest in the international healthcare environment and direct experience in multiple countries Eligible to work in role location without visa sponsorship Fluency in English both verbal and written  Why Join? Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. At IQVIA, you will have access to the most cutting-edge technology, the largest data sets, the best analytics tools and, in our opinion, some of the finest minds in the Healthcare industry. You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1058828
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07.03.2020

IQVIA AG

Senior Consultant - Technology Solutions - Pharma & Healthcare

  • IQVIA AG

  • 4040Basel, CH

  • 07.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. The Technology Solutions Team of IQVIA focuses on bringing innovative solutions to headquarter and local clients in order to strengthen their competitive positioning through advanced insights and greater commercial efficiency. Are you interested in strengthening our team with your expertise of Multi-Channel-Management (MCM) and Social Media solutions to create value add for our clients in an international environment? Your Tasks: Support the Engagement Managers to execute multi-channel management projects both in technical implementation and business consulting. Lead workstreams in consulting or technology implementation projects with regards to Multi-Channel-Management and Social Media. Support Engagement Managers and Principals in business development activities across our technology service portfolio. Support further development of Multi-Channel-Management and Social Media offerings. Effective client communication. On-site client engagement and project execution. Travel across countries and work with different teams in a dynamic environment, adhere to strict deadlines and multiple projects to deal with. Your Profile: Master degree or equivalent in business administration, computer science or related discipline, or knowledge acquired through equivalent experience. First experiences in commercial business in pharma / healthcare industry – ideally with experience in Multi-Channel-Management, KOL Management, CRM, Social Media. Good understanding of commercial customer engagement concepts in pharmaceutical industry. Ability to bridge technology and business requirements from our clients in Multi-Channel-Management and Social Media. Proven track record in project work and first experiences in leading (sub) streams in larger client projects. Fluency in English is a must. Strong commitment to effective, cross-functional teamwork. Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1107887
Inserat ansehen

06.03.2020

IQVIA AG

(Senior) Principal - Consulting Services, Pharma And Healthcare Industry

  • IQVIA AG

  • 4051Basel, CH

  • 06.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Individuals joining us are assured of a rewarding and progressive career in life sciences consulting. You’ll have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in delivering solutions.  We operate in a truly multi-cultural, collegial and collaborative work environment that is rich in development and growth. Role As a (Senior) Principal within Consulting Services , you will take on a variety of roles that focus primarily within the following core areas: client/project leadership, business development, and firm/operational leadership roles. The main focus of a principal is to deliver outstanding client service, while building trusted relationships with new and existing clients that enhance the Consulting Services brand. The principal’s success will be measured by the ability to take on larger and more complex projects, while opening up new business relationships to the firm. You will work directly with clients to develop business opportunities and deliver projects ensuring that delivery results are at high levels of client satisfaction. Responsibilities Develop and deliver insightful, value-added strategies that address complex client issues. Create and elevate new business opportunities through the identification of value-added follow-on work and identify new revenue opportunities with existing and new client organisations. Act as principal owner of client engagements; ultimate responsibility for client satisfaction and delivering high levels of quality/added value. Provide follow-up with clients after project deliverables have been completed to ensure client satisfaction. Allocate direction, advice, and intellectual leadership to clients and delivery teams. Provide high level input and ensure development of client reports and presentations. Ability to deliver all or significant portions of findings to clients. Lead thought leadership and firm building initiatives. Remain current on industry, clients, and competitive trends and directions in order to anticipate and identify new business challenges and issues with assigned clients. Contribute to the enhanced awareness of Consulting Services in the marketplace, e.g. through speaking engagements, client meetings, and publications. Participate in annual performance review team processes. Engage in recruitment and selection of new staff. Mentor, coach, and share subject matter expertise with others to help develop individuals and capabilities delivering world-class solutions for clients. Skills & Experience The successful candidate will have a track record of success across the majority of the following competencies: A minimum of a Master’s degree or equivalent in business administration, health economics or related discipline, or knowledge acquired through equivalent experience. Extensive experience in the Life Science, Pharma, Healthcare or consulting industry. Principal owner of client engagements to the brand and commercial functions within leading Life Sciences organizations, focused on client satisfaction and outstanding client deliverables. Proven capability to identify new revenue opportunities with existing clients. Proven skills in identifying, recruiting, mentoring/coaching, and retaining top talent for Consulting Services practice teams. Proven success selling complex strategy and operations engagements to the top Pharma/Life Sciences companies. Actively participate in proposal development and ongoing pre-sales meetings with potential new client organizations. Proven ability to build relationships, identify client pain points, and develop custom solutions at the CEO/COO/CMO level (ideally providing comprehensive and authoritative knowledge in brand/commercial services solutions demonstrated through speaking, writing, and general eminence). Has the experience to craft client brand and commercial strategies that are specific with regard to international geography. Fluency in English is a must, any other language is of advantage. Strong commitment to effective, cross-functional teamwork. Expertise in Pricing and Market Access would be highly beneficial. Location: Basel, Switzerland Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1074790
Inserat ansehen

01.03.2020

IQVIA AG

Consultant - Consulting Services, Pharma and Healthcare Industry

  • IQVIA AG

  • 4040Basel, CH

  • 01.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Overview  Consulting Services is the world’s leading, specialized advisor on critical business issues in the life sciences. We are the strategy arm of IQVIA, a leading provider of information, services and technology for the healthcare industry in 100+ countries around the world. Our Consulting Services team offer end-to-end management consulting in key issues areas that include: business unit, therapy area, brand strategy, portfolio strategy, launch strategy, pricing & market access, and commercial model design and optimization.  Individuals joining us are assured of a rewarding career in life sciences consulting, replete with opportunities to address diverse and challenging client problems, travel on cross-geography projects, interact with senior client leaders and gain exposure to a truly multicultural and collaborative work environment. We are looking for a Consultant to join our Team! Start date: as soon as possible. Role & Responsibilities  As a Consultant , you’ll be responsible for managing small teams in the design, development and delivery of medium sized- consulting projects as well as components of larger and complex projects. Your analytical, inter-personal, creative thinking, business management and leadership skills will be called upon from day one. You will help create change in the world of Life Sciences, every project will be different but a sample of the things you can expect to accomplish are:  Conducting primary and secondary research and performing quantitative and qualitative analysis to identify key client issues, translating the data into meaningful insights and communicating recommendations to key decision makers.  Leveraging business experience and acumen in identifying strategic alternatives to client questions.  Working in a team of like-minded professionals to create reports, presentations, workshops with client employees, management teams and other stakeholders, under the guidance our “the best on the business” team leaders.  Developing broad knowledge of related consulting methodologies and pharmaceutical market through the delivery of consulting engagements and participation in formal and informal learning opportunities.   Managing the execution of client projects; develop a plan to implement the strategic recommendations and working closely with clients.   Assisting with key business proposals and business development initiatives. Leading learning, development and recruiting programs.  To reward you for your hard work you will have the chance to travel globally, establish influential connections, receive world-class training, unparalleled career-development and of course, financial- which is second to none!  About You  Candidates interested joining as a Consultant should have:  A strong academic record including an MBA from a top business/research school and a relevant life-sciences background OR and an experienced professional with extensive proven experience of delivering commercial pharmaceutical projects at a global level   Demonstrable analytical, interpretative and problem-solving skills  Well-developed written and verbal communication skills including presentations, meeting and workshop facilitation, business and report writing Strong capability in juggling priorities to meet deadlines while retaining consistently high quality outcomes Excellent interpersonal skills and ability to work effectively with others in and across the organization to accomplish team goals  Knowledge of key issues and current developments in the pharmaceutical and healthcare industries is desirable but not required Prior experience or avid interest in the healthcare and life sciences industries Some experience managing projects  Knowledge of consulting methodologies, tools and techniques are desirable  Adaptability and an ability to learn quickly and apply new knowledge  A willingness and ability to travel  Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1056110
Inserat ansehen

19.03.2020

IQVIA AG

Clinical Research Associate II

  • IQVIA AG

  • 8044Zurich, CH

  • 19.03.2020

  • Vollzeitstelle

Job Description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. RESPONSIBILITIES: Study Planning Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation for trial inclusion. Assume ambassadorial role to facilitate communication between sites and Novartis CPO to increase value proposition to investigators. Facilitate the preparation and collection of site and country level documents during all phases of the trial. Supports the CSM in the oversight of Country and Site Trial Master Files (TMF). During all phases of the trial ensure archiving per relevant SOP. Negotiate investigator remuneration; prepare financial contracts between Novartis and investigational sites and investigators. Ensure adherence to payment schedule. Study Start-up Execute site initiation and training, generate initiation visit report. Study Execution Implement complete site management including monitoring visits, regulatory assessment, drug supply management, etc. to ensure compliance with protocol, GCP, global and local regulations, global and local processes. Identify problems at sites; resolve issues and escalate as appropriate. Collaborate with the CSM to ensure recruitment and execute contingency plans, as needed. Complete preparation and generation of visit monitoring reports as per relevant SOP Review and manage data at site; resolve technical and content issues on a continuous basis in order to achieve timely database lock targets. If working with central CRAs (blinded and un-blinded), respond to alerts and follow-up to ensure resolution of issues Study Close-out Implement site close-out activities and generate site close-out report. Provide feedback on site performance for future trial site feasibility/selection General Improve skills by timely completion performance of assigned global and local training. REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Good knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Strong therapeutic and protocol knowledge as provided in company training Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer Strong written and verbal communication skills including good command of English language Strong organizational and problem-solving skills Effective time management skills Ability to establish and maintain effective working relationships with coworkers, managers and clients MINIMUM REQUIRED EDUCATION AND EXPERIENCE Bachelor's degree in a health care or other scientific discipline or educational equivalent and 1 year of on-site monitoring experience; or equivalent combination of education, training and experience Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients. Forge a career with greater purpose, make an impact, and never stop learning. Job ID: R1123688
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