Regulatory Affairs Jobs in France

Responsible for leading and executing regional and global regulatory strategies to support drug and device development. This role ensures compliance with European and international regulations while enabling efficient clinical development and successful

This Expert Level role provides on‑site regulatory leadership with a strong manufacturing focus, ensuring regulatory considerations are embedded early into site initiatives and day‑to‑day operations. This leader interacts closely with global and

Lead and execute the country/regional Medical Affairs strategy, representing the medical function internally and externally, including interactions with health authorities and cross‑functional teams. Build and maintain strategic scientific partnerships

The scientific and strategic leader of oncology drug discovery programs, accountable for driving projects from early concept to Preclinical Candidate (PCC) nomination, in alignment with Oncology Therapeutic Area and R&D strategy. As the integrator of

Understands and keeps updated with the pre-clinical, clinical pharmacology and data relevant to the molecule of interest. Knowledge on antibody is a plus; Critically reads and evaluates relevant medical literature with deep understanding of the data and