Our client, a fast-growing international CRO with over 35 years of experience, is seeking a ScientificDirector / Clinical Pharmacologist to support its early-phase clinical activities in France and globally.This role will lead scientific input across clinical pharmacology studies, ensuring scientific integrity, regulatory compliance, and study optimisation.
You’ll work closely with cross-functional teams and clients to shape study design, protocols, and development strategies.Key Responsibilities:
Serve as scientific and medical lead on early-phase clinical studiesDraft/validate study synopses, protocols, and CSRsSupport risk mitigation and compliance across clinical activitiesAdvise across other areas (biostats, central lab, non-clinical)Contribute to business development proposals and client engagementIdeal Background:
Medical degree, ideally with PhD in pharmacokinetics, pharmacology, or biostats5+ years’ experience in clinical pharmacology/early developmentStrong knowledge of PK/PD, safety pharmacology, EMA/FDA guidelines, and GCPFluent in EnglishStrong leadership, collaboration, and multitasking skills HartmannYoung Rennes35000 Autre(s) 0 mois
