Associate Director / Director - Medical Writing, Oncology
Treeline Biosciences · Any Office
Posted 28 days ago · $164,450 to $224,787
or apply directly on Treeline Biosciences's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 28 days Treeline Biosciences's roles stay open a median of 45 days
- Reposted
- No
- Salary listed
- Yes 100% of Treeline Biosciences's roles list one
- Ghost-job risk at Treeline Biosciences
- high 8 stale, 0 reposted of 15 open
- Hiring momentum
- 19 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Treeline Biosciences's own greenhouse board since 2026-08-03. Full hiring picture for Treeline Biosciences.
About this role
The Associate Director / Director of Medical Writing in Oncology is responsible for authoring and coordinating high-quality regulatory and clinical documents for oncology development programs. This role involves close collaboration with cross-functional teams to ensure documents are accurate, compliant, and submission-ready, while also managing timelines and quality control. The ideal candidate will have extensive experience in oncology medical writing and be comfortable working independently on complex documents.
- benefits
- 1/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 5/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Treeline Biosciences as an employer.
What you need
- Bachelor's degree in life sciences
- 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)
- Strong knowledge of ICH guidelines (E3, E6, M4/CTD format)
- Excellent scientific writing skills
Nice to have
- Experience with additional oncology-specific regulatory pathways (e.g., accelerated approval, breakthrough therapy designation, orphan drug designation)
- Experience authoring documents listed above
- Familiarity with document management systems
- Prior experience in a small or growing biotech
Worth weighing
- No specific benefits listed
- Salary range provided but may vary based on experience and location
- Role requires strong independence and ability to manage multiple documents under time pressure
Summarised from Treeline Biosciences's posting. Read the full original.
Listed by Treeline Biosciences on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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