Interim VP, Regulatory Affairs
About the role
For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise‑build‑operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end‑to‑end suite of fully customizable consulting solutions that de‑risk and accelerate our partners’ most high‑profile drug and device programs.
Interim VP, Regulatory Affairs – Interim VP‑level Regulatory Affairs consultant to provide senior strategic and hands‑on support.
Responsibilities
- Set regulatory priorities across development programs
- Lead preparation for FDA interactions and key submissions
- Advise cross‑functional teams on regulatory decisions
- Provide oversight to keep work moving during a period of limited team capacity
Schedule
- 20 hours per week
- Hybrid schedule (onsite work in Berkeley Heights, NJ)
- Minimal travel
- 4 months in duration