Senior Manager Regulatory Affairs
Travere Therapeutics
Travere Therapeutics is seeking an Associate Director of CMC Regulatory Affairs to provide strategic regulatory leadership for biologics across development and commercial programs. The role focuses on late-stage development, Phase 3, and rare disease therapeutics, coordinating with multiple functions to align CMC plans with global requirements. The position demands extensive experience with biologics, INDs/NDAs, and post-approval changes, with responsibility for submissions, risk assessment, and #J-18808-Ljbffr
Vacancy posted 2 hours ago
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