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Job description
Treeline Biosciences is seeking an Associate Director / Director, Medical Writing in Oncology to author and coordinate high-quality regulatory and clinical documents across the product lifecycle. You will own documents end-to-end and coordinate with Regulatory, Clinical Development, Biostatistics, and vendors to ensure submission-ready quality.
The role requires 8+ years of oncology regulatory writing experience, strong scientific writing, and the ability to work independently while guiding
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Worksite address
watertown, MA, 02472, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.