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24.11.2021

Global Safety Officer M/F

  • Switzerland
  • Festanstellung 100% | Management / Kader

  • Merken
  • drucken

Global Safety Officer M/F

Poste prioritairement réservé aux salariés SARD appartenant soit à une catégorie professionnelle impactée par des suppressions, et/ou des transferts hors bassin d’emploi, au sein d’une direction elle-même impactée par des suppressions de postes, soit à l’établissement de Strasbourg.

Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l’international, l'anglais étant la langue de travail.

The GSO is the safety expert and safety lead for Sanofi products.

KEY ACCOUNTABILITIES

Internal & External Safety Expert

  • Provide PV and risk management expertise to internal and external customers
  • Safety expert for product
  • Maintain knowledge of product, product environment, and recent literature
  • Maintain PV expertise, and understanding of international safety regulations and guidelines
  • Lead cross functional Safety Management Teams (SMTs)
  • Communicate with and represent PV analyses and PV position within project/product teams, in safety governance and benefit-risk governance activities and committees (e.g. Safety Management Committee, Benefit-Risk Assessment Committee), with external partners, key opinion leaders, and Health Authorities, and during internal and external negotiations
  • Provide strategic and proactive safety input into development plans
  • Support due diligence activities and pharmacovigilance agreements

Signal Detection & Assessment

  • Responsible for signal detection and analysis
  • Collaborate with Center of Excellence for Signal Detection and Data Mining and Safety Epidemiology group
  • Identify and implement proactive safety analysis strategies to further define the safety profile
  • Lead aggregate safety data review activities and coordinate safety surveillance activities

Risk Assessment & Risk Management & Benefit-Risk Assessment

  • Provide proactive risk assessment
  • Co-lead benefit-risk assessment with other relevant functions
  • Develop risk management strategies and plans and monitor effectiveness
  • Collaborate with Center of Excellence for Risk Management and Epidemiology/Benefit-Risk groups

Submission Activities

  • Represent safety position in cross functional submission teams
  • Ensure generation, consistency, and quality of safety sections in submission documents
  • Write responses or contributions to health authorities’ questions
  • Support preparation and conduct of Advisory Committee meetings

Report Writing

  • Document, contribute to, coordinate, review and/or validate Periodic Reports, e.g.: RMP update, IND Annual Report, Annual Safety Report/Development Safety Update Report, Periodic Safety Update Report
  • Serve as the medical safety expert to the GPV Periodic Reports group for assigned projects and products

PROFILE

Knowledge & Skills

  • Excellent clinical judgment
  • Capability to synthesize and critically analyze data from multiple sources
  • Ability to communicate complex clinical issues and analysis orally and in writing
  • Able to develop and document sound risk assessment
  • Demonstrates initiative and capacity to work under pressure
  • Demonstrates leadership within cross-functional team environment
  • Excellent teamwork and interpersonal skills are required
  • Fluent in English (written and spoken)

Formal Education & Experience Required

  • M.D. Degree, or degree in pharmacy, biological sciences or related disciplines
  • Non-MD GSO can only be assigned to the following product areas: generics, consumer healthcare, vaccines and “mature products”, where mature products are defined as those no longer under patent or other data exclusivity protection AND where there is no on-going significant investment in development or marketing
  • For MD, Board Certified/Board eligible, or equivalent, is preferred; For other degrees, advanced post-graduate qualifications e.g. Master or PhD are preferred
  • For M.D., minimum 3 years' and for other degrees, minimum 5 years' total experience in international pharmacovigilance, or equivalent relevant industry experience (e.g. clinical development) with relevant clinical experience considered. Exceptionally, candidates may be considered if they have proven excellence in a similar prior position, even if they have less than 3 years international PV experience

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

As part of its diversity commitment, Sanofi is welcoming and integrating people with disabilities.

Arbeitsort:

Switzerland

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