Regulatory Affairs Manager
Travere Therapeutics
Travere Therapeutics is seeking an Associate Director, Regulatory Project Manager to lead global regulatory programs from planning to submissions. The role partners with Regulatory Leads and other functions to drive timelines, dashboards, and delivery of high-quality regulatory documents in a fast-paced, patient-focused environment. The ideal candidate has 8+ years in biotech/pharma PM, a strong background in global regulatory affairs, and PMP certification preferred. #J-18808-Ljbffr
Vacancy posted 1 day ago
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