VP, Regulatory Affairs — Rare Disease & Accelerated Pathways

A clinical-stage biopharmaceutical company in Switzerland is seeking a VP of Regulatory Affairs to lead strategic regulatory initiatives. The ideal candidate will have over 15 years of experience in regulatory affairs, with a focus on early clinical development, particularly in the context of rare genetic diseases. This role involves defining global regulatory strategies, leading FDA interactions, and overseeing regulatory submissions. Competitive compensation and benefits are offered, including a flexible PTO policy and rapid career advancement for strong performers. #J-18808-Ljbffr