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Interim, VP, Regulatory Affairs

ProPharma

Job Description

Interim VP, Regulatory Affairs

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  • Interim VP-level Regulatory Affairs consultant to provide senior strategic and hands-on support.
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  • 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.
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  • 20 hours per week
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  • Hybrid Schedule (onsite work in Berkeley Heights, NJ)
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  • Minimal travel
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  • 4 months in duration
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Vacancy posted 15 days ago
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