Manager, Pharmacovigilance and Medical Information

Who You Are:

You are an experienced Pharmacovigilance professional with strong scientific judgment and a thorough understanding of the French and European regulatory environment. You are comfortable balancing operational responsibilities with oversight, governance and cross-functional collaboration.

You communicate clearly with a broad range of stakeholders and are able to evaluate complex scientific information, identify potential safety risks and translate regulatory requirements into effective operational processes. You are rigorous and detail-oriented while remaining proactive, pragmatic and adaptable in a dynamic international environment.

Required Skills:

• Strong knowledge of French and EU pharmacovigilance regulations and Good Pharmacovigilance Practices (GVP).
• Demonstrated experience in pharmacovigilance and medical information.
• Ability to assess safety information, benefit-risk considerations and potential product quality concerns.
• Experience with pharmacovigilance case management, documentation and safety databases.
• Ability to evaluate and interpret complex medical and scientific information.
• Strong understanding of PV quality and compliance requirements, including audit and inspection readiness.
• Excellent organizational skills, attention to detail and ability to ensure appropriate documentation, follow-up and archiving.
• Strong communication and stakeholder management skills, with the ability to work effectively in multidisciplinary and cross-functional teams.
• Ability to operate effectively with global teams, external partners and vendors.
• Proactive, adaptable, agile and responsive approach.
• Fluent in French and strong written scientific English, with the ability to read and prepare scientific documents, reports and communications.

Expected Educational Background:

• Pharm.D or M.D.
• Minimum 4 years of professional experience in Pharmacovigilance and Medical Information.

Additional Employment Conditions:

• Position based in France.
• Hybrid working model.
• The role combines approximately 50% global biosimilars Pharmacovigilance activities and 50% Biogen France Pharmacovigilance and Medical Information activities.

Job Level: Management

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.