Travere Therapeutics is looking for an Associate Director, Medical Writing who will oversee regulatory submissions and lead medical writing projects. The ideal candidate will have a Master's degree in Life Sciences, with at least six years of progressively responsible experience in medical writing, especially in the biopharmaceutical sector.
This role involves collaboration with cross-functional teams, ensuring that all documents meet quality and regulatory standards. A competitive compensation package is available, along with comprehensive benefits.
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This position is listed as full time and onsite.