VP, Regulatory Affairs

Interim VP, Regulatory Affairs Interim VP-level Regulatory Affairs consultant to provide senior strategic and hands-on support. The consultant will help set regulatory priorities across development programs, lead preparation for FDA interactions and key submissions, advise cross-functional teams on regulatory decisions, and provide oversight to keep work moving during a period of limited team capacity.20 hours per week Hybrid Schedule (onsite work in Berkeley Heights, NJ) Minimal travel 4 months in duration