Travere Therapeutics seeks an Associate Director, Medical Writing responsible for overseeing regulatory submissions and authoring critical documents. This role leads medical writing projects and ensures compliance with regulatory standards while mentoring junior writers.
Candidates should have a Master’s degree and a minimum of 6 years in medical writing within the biopharmaceutical industry. Strong writing, editing, and project management skills are essential. Remote working options are available, with a competitive salary range of $150,000 - $195,000.
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