Associate Director, Project Manager - Regulatory Affairs

Role: Associate Director, Regulatory Project Manager at Travere Therapeutics, leading global regulatory activities to ensure compliance and support submissions for rare disease therapies. Responsibilities: develop and manage integrated regulatory timelines, facilitate cross-functional collaboration across departments (Regulatory Affairs, Clinical Development, CMC, Quality, Commercial), oversee submission planning (INDs, NDAs, BLAs, post-marketing reports), track milestones, and support agency interactions. Drive process improvements and mentor team members. Requirements: Bachelor’s degree in Life Sciences or related, 8+ years of project management experience in biotech/pharma, with regulatory project management preferred; PMP certification highly desired. High-Value: rare disease therapies, global regulatory submissions, lifecycle management, cross-functional coordination, experience with regulatory tools (e.g., Smartsheets, MS Project). WorkSetup: remote in San Diego with less than 10% travel domestically and internationally.