Senior Regulatory Project Manager — Global Submissions
Travere Therapeutics
Travere Therapeutics in San Diego, CA, is seeking an Associate Director, Regulatory Project Manager to lead global regulatory activities for rare disease therapies. You will coordinate cross-functional teams, manage submission timelines, and drive regulatory strategies to meet health authority requirements. The role emphasizes collaboration with Regulatory Affairs Strategy, Regulatory Operations, Clinical Development, and external partners. #J-18808-Ljbffr Travere Therapeutics
Vacancy posted 4 days ago
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