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Cécile is a pharmacist with post-graduation in Drug Development and Clinical Research, in Statistics applied to Clinical Research, complemented with a master in Regulatory Affairs. She has 15+ years of consultancy experience in the pharmaceutical industry sector, combining experience from both the clinical development and market access side. She has been involved in multiple projects for a variety of health products, including orphan drugs, ATMPs, oncology products, vaccines, biosimilar products, repurposed medicines, medical devices and diagnostics, and medical procedures. Her field of expertise encompasses broad range of market access projects, including market access strategy at early, pre-and post-launch phases, payer/HTA value communication, HTA dossiers, HTA advice, clinical development, regulatory processes, and health policies. Prior joining Putnam PHMR, she was working in a consultancy supporting the set-up of clinical research studies in various therapeutic areas and regulatory intelligence activities in France.