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Senior Clinical Project Lead — Global Trials & Regulatory

Description

Design, implementation and coordination of clinical studies with the support of Clinical Operations, Pharmacovigilance, Biometrics and Medical Writing: Plan the clinical development program Prepare studies protocols, amendments and reports Prepare regulatory dossiers Manage relationships with investigators and opinion leaders

Requirements

Holder of additional training in methodology (CESAM, IUD, …) Successful experience of Clinical Project Manager in a pharmaceutical company or CRO 6-8 year’s e…

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