What are the responsibilities and job description for the Interim, VP, Regulatory Affairs position at ProPharma?
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