Clinical development, Regulatory and market access
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15 years of experience in global clinical development (Phase 1 to 4 and EAP) incluidng 3 years in market access.
International experience in both pharma and biotech companies (EU, US, Brazil..)
Expertise in clinical trial regulations and market access in France and internationally (FDA, EMA)
Proven leader in driving market strategies and accelertaing treatment approvals with a strong focus on innovative solutions and cross-functional collaboration.
Master I and II in oncopharmacology and Executive master in strategy and management of health industries (ESSEC business school)