Global Regulatory Project Lead
Travere Therapeutics
Travere Therapeutics is seeking an Associate Director, Regulatory Project Manager to lead global regulatory activities for rare disease therapies. You will drive timelines, submissions, and cross‑functional collaboration across Regulatory Affairs, Clinical Development, and Quality to ensure timely delivery and inspection readiness. The role focuses on coordinating cross‑functional teams, building regulatory dashboards, and managing key milestones across product lifecycles in a fast‑paced #J-18808-Ljbffr Travere Therapeutics
Vacancy posted 2 days ago
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