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Job description
Travere Therapeutics in San Diego is seeking an Associate Director, Regulatory Project Manager to lead global regulatory affairs activities for rare disease programs. You will coordinate timelines, cross‑functional teams, and submission plans to meet health authority requirements in a fast-paced, patient‑focused environment.
The role requires 8+ years of biotech/pharma project management, a life sciences degree (MS/PhD preferred), PMP preferred, and experience with Smartsheets or MS Project.
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Worksite address
san diego, CA, 92189, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.