AbCellera seeks a Senior Medical Writer to develop regulatory and clinical documents supporting antibody-based drug programs. The role requires extensive experience preparing nonclinical and clinical submissions, collaborating across functional teams, and maintaining expertise in evolving regulatory standards.

Prepare clinical and regulatory documents including Module 2-5, briefing books, safety updates, and agency responses

Organize document review meetings and partner with project teams on authoring strategy

Manage multiple concurrent projects while aligning deliverables and timelines across teams

Lead adoption of AI-assisted writing tools to improve document preparation efficiency

8+ years medical writing experience in pharma or biotech

- Expertise writing clinical and regulatory documents per ICH, GCP guidelines
- Advanced knowledge of drug development, clinical research, and biostatistics
- Solid cross-functional collaboration and project management skills
- Compensation: CAD $118,000–$150,000 base annually

📌 Senior Medical Writer - Biotechnology (Vancouver)
🏢 AbCellera
📍 Vancouver