Interim VP, Regulatory Affairs Job at ProPharma Group, United States

  • ProPharma Group
  • United States

Job Description

ProPharma Group seeks an interim VP-level regulatory affairs consultant to provide strategic guidance and operational support for 4 months at 20 hours weekly. The role involves setting regulatory priorities, leading FDA interactions, and advising cross-functional teams during a period of constrained capacity.

Responsibilities

  • Establish regulatory priorities across active development programs
  • Lead preparation and strategy for FDA meetings and key submissions
  • Provide senior-level regulatory guidance to cross-functional teams
  • Oversee regulatory workstreams to maintain progress and momentum

Requirements

  • VP-level experience in regulatory affairs
  • Strategic expertise in drug or device regulatory pathways
  • Experience preparing FDA submissions and interactions
  • Ability to advise cross-functional teams on regulatory strategy
  • Availability for hybrid work in Berkeley Heights, NJ area

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