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Job description
Pliant Therapeutics is seeking a Vice President, Regulatory Affairs & Quality (GxP) to lead an integrated regulatory and quality function for an oncology portfolio, including Phase 1b assets. This hands-on leader will partner with FDA and global authorities, shape strategy, and scale QMS across GLP, GCP, GVP, and GMP in a development-stage setting.
The role is hybrid (3 days onsite per week in South San Francisco) with accountability for strategy, execution, and cross-functional collaboration at
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Worksite address
south san francisco, CA, 94083, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.