# Associate Director / Director - Medical Writing, Oncology at Treeline Biosciences

- Company: Treeline Biosciences
- What the company does: Backed by GV.
- Company website: https://treeline.bio
- Type: Startups
- Level: Principal and up
- Location: Any Office
- Work setup: On-site
- Pay: $164K to $225K base salary per year (USD)
- Posted: 2026-08-19
- Apply by: 2026-10-08
- Apply: https://job-boards.greenhouse.io/treelinebiosciences/jobs/6147410004
- Page: https://www.1752.vc/careers/jobs/treeline-biosciences-associate-director-director-medical-writing-oncology/

## About the role

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.

## What they're looking for

- Bachelor's degree in life sciences required, advanced degree (PhD, PharmD, MS) strongly preferred
- 8+ years of regulatory/medical writing experience, with a significant portion in oncology drug development
- Direct, hands-on experience authoring clinical and regulatory oncology submissions and/or amendments
- Experience supporting responses to health authority inquiries (FDA and/or ex-US agencies), including briefing documents for regulatory meetings
- Strong knowledge of ICH guidelines (E3, E6, M4/CTD format) and regulatory document standards
- Excellent scientific writing skills with the ability to synthesize complex clinical and nonclinical data into clear, accurate, well-organized documents

Tags: Regulatory