Cécile Antolin is an Associate Director Regulatory Medical Writer at Pierre Fabre Group, where they are responsible for supporting regulatory documents and dossiers for oncology products. They previously served as a Medical Writing Leader at Servier, overseeing regulatory deliverables and managing a team of medical writers. Cécile began their career as a Medical Coding Officer in Pharmacovigilance at Sanofi and holds a PharmD and PhD in Pharmacology from Université Paris-Sud and Université Paris Cité, respectively.
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