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Interim, VP, Regulatory Affairs

ProPharma

Interim VP, Regulatory Affairs

Scroll down the page to see all associated job requirements, and any responsibilities successful candidates can expect.

  • 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 xhyhwjd hours per week
  • Hybrid Schedule (onsite work in Berkeley Heights, NJ)
  • Minimal travel
  • 4 months in duration

Vacancy posted 6 days ago
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