Europe CMC Regulatory Director – Oncology

Headcount is seeking a Director of Regulatory Affairs CMC Europe to lead the regulatory strategy for novel small-molecule therapies in oncology. This role requires steering global CMC development, submissions and lifecycle management across clinical, regulatory and manufacturing functions, with a focus on Module 3 and interactions with FDA/EMA.The candidate will collaborate across Development, Quality and Supply Chain to ensure timely, successful global submissions while shaping the strategy #J-18808-Ljbffr