Global Regulatory Submissions — Associate Director

A specialized regulatory consulting firm in New Jersey is seeking an Associate Director of Regulatory Affairs to lead global submissions. The successful candidate will drive strategic oversight and operational leadership, ensuring compliance with FDA, EMA, and global regulatory requirements. Ideal candidates will have 7-10 years of regulatory experience and a strong grasp of submission management across the drug development lifecycle. This role requires excellent communication skills and the ability to thrive in a fast-paced environment. #J-18808-Ljbffr