Interim VP, Regulatory Affairs
ProPharma seeks an Interim VP-level Regulatory Affairs consultant to provide senior strategic and hands-on support for 4 months at 20 hours per week on a hybrid basis. The consultant will set regulatory priorities across development programs, lead FDA interaction preparation and key submissions, advise cross-functional teams on regulatory decisions, and provide oversight during a period of limited team capacity. ProPharma provides consulting across regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology for biotech, med device, and pharmaceutical organizations.
- •Help 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
Found on fractionaljobs.io. Link checked Nov 9. Marquee links to the company's own application. We are not the employer.