Treeline

Associate Director / Director, Medical Writing, Oncology Position Summary This is a hands-on, individual-contributor role responsible for authoring and coordinating high-quality regulatory and clinical documents in support of the company's oncology development programs. This role partners closely with the SVP, Development and Regulatory Strategy and cross-functional teams (Clinical, Biostatistics, Nonclinical, CMC, Regulatory) to prepare, format, and QC, submission-ready clinical and regulatory documents across the product lifecycle. The ideal candidate is a strong, independent oncology medical writer who is comfortable owning documents end-to-end - from outline through final QC. The specific title and level will be determined based on the selected candidate's depth of oncology and regulatory writing experience. We are seeking someone with 8+ years of regulatory/medical writing experience, with substantial oncology medical writing experience. The candidate should be able to...