Global PV & Local Medical Information Manager – France

Biogen, Inc.; Paris; Hybride; EUR 110 000 - 140 000; Plein temps

Avantages offerts par ce poste

Hybrid work model

Résumé du poste

Biogen France seeks a Manager, Pharmacovigilance & Medical Information to oversee global PV activities for biosimilars in partnership with Samsung Bioepis and to manage local PV and Medical Information activities for Biogen France. You will collaborate with local and global teams, health authorities, healthcare professionals, patients and vendors to ensure patient safety and regulatory compliance.

This hybrid role combines governance, process development, and training across both global

Qualifications

• Pharmacovigilance and Medical Information experience.
• Fluent in French and strong written English.
• Minimum 4 years of PV/Medical Information experience.
• Hybrid working model in France.

Responsabilités

• Provide oversight of global PV activities for biosimilars in accordance with PVAs.
• Collaborate with Biogen France PV Responsible Person, Biogen EU QPPV and Samsung Bioepis EU QPPV.
• Develop, improve and implement regional and local PV processes and documentation.
• Oversee PV activities related to Organised Data Collection Programs (ODCPs) for biosimilars.
• Support local signal detection and management of reports for French Health Authorities.
• Oversee local PV vendors and PV requirements within commercial and non-commercial agreements.
• Develop and deliver PV training for Biogen France employees and relevant external partners.

Connaissances

Pharmacovigilance

Medical Information

GVP knowledge

Regulatory compliance

Safety signals

Formation

Pharm.D or M.D.

Description du poste

Biogen France seeks a Manager, Pharmacovigilance & Medical Information to oversee global PV activities for biosimilars in partnership with Samsung Bioepis and to manage local PV and Medical Information activities for Biogen France. You will collaborate with local and global teams, health authorities, healthcare professionals, patients and vendors to ensure patient safety and regulatory compliance.

This hybrid role combines governance, process development, and training across both global