Senior Medical Writing Lead - Regulatory Submissions

Travere Therapeutics is seeking an Associate Director of Medical Writing to lead regulatory submission efforts, ensuring adherence to quality and strategic oversight. The role requires collaboration with cross-functional teams and involves authoring a range of regulatory documents.

Ideal candidates possess a Master's degree in Life Science and extensive experience in medical writing, with a strong focus on detailed communication and project management skills. Join our mission to develop life-changing therapies for patients with rare diseases.