Senior Regulatory Affairs Lead - Global Submissions

A pharmaceutical firm is seeking a Senior Director of Regulatory Affairs to provide strategic leadership and ensure compliance with regulatory requirements. You will oversee regulatory activities, lead teams, and develop comprehensive strategies for drug product development. The ideal candidate has at least 10 years of pharmaceutical experience, strong project management skills, and global regulatory management experience. This position is full-time with a preference for a New Jersey home office and includes hybrid work options. #J-18808-Ljbffr