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