Senior Regulatory Affairs Lead: FDA Submissions & Compliance

A leading global clinical research organization is seeking a Senior Regulatory Affairs Associate in Jefferson City, Missouri. The ideal candidate will bring 3–5+ years of regulatory experience and strong project management skills. Responsibilities include ensuring compliance with FDA regulations, preparing regulatory submissions, and collaborating with internal teams to mitigate regulatory impacts. This position offers a dynamic work environment focused on product launches and lifecycle management. Candidates with advanced degrees in natural sciences or legal affairs are preferred. #J-18808-Ljbffr