Director, Regulatory Affairs

Travere Therapeutics is seeking a Manager of Regulatory Affairs Strategy to drive regulatory leadership for late-stage development programs and oversee global submission planning from development through lifecycle management. The role requires strong regulatory knowledge, cross-functional teamwork, and the ability to manage complex submission timelines. The position involves collaboration with clinical, nonclinical, CMC, regulatory operations, medical writing, and project management teams in a #J-18808-Ljbffr