Director, Regulatory Strategy & Submissions

A pharmaceutical company based in New Jersey is seeking a Director of Regulatory Affairs to execute the regulatory strategy across development and commercial product portfolios. Responsibilities include overseeing regulatory submissions to the FDA, providing leadership in regulatory planning, and managing day-to-day operations. Candidates should have over 10 years of relevant experience with substantial knowledge of the drug development lifecycle. The role demands strong leadership and project management skills in a compliance-focused environment. #J-18808-Ljbffr