Senior Regulatory Affairs Manager
Travere Therapeutics
Travere Therapeutics in San Diego, remote optional, is seeking an Associate Director, Regulatory Project Manager to lead and coordinate global regulatory activities for rare-disease therapies. You will manage timelines, cross-functional collaboration, and submissions to health authorities while supporting program strategy and compliance. This role requires a strong background in regulatory project management, 8+ years in biotech/pharma, and PMP certification is preferred. #J-18808-Ljbffr
Vacancy posted 5 days ago
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