CMC Regulatory Director, Global Submissions & Strategy

A pharmaceutical company is seeking an Associate Director of Regulatory Affairs – CMC in Morrisville, NC. This role involves preparing and managing regulatory CMC submissions for clinical development and ensuring compliance with global standards. Candidates should have approximately 8 years of experience, strong leadership in regulatory matters, and the ability to collaborate across teams. The position offers a competitive compensation package and a hybrid working model, requiring 2-3 days in the office weekly. #J-18808-Ljbffr