Senior Medical Writer
Each of us cares about someone who will need medicines. That’s why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients that need them. We pursue truth and scientific rigour and have the courage to work at the edge of the unknown.
We are looking for a skilled, detail-oriented Senior Medical Writer with extensive experience contributing to nonclinical, clinical, and regulatory affairs teams in a dynamic industry setting. You will be responsible for delivering high-impact regulatory documents that advance our programs and support our mission to bring new therapies to patients. If you are a writer who takes pride in turning complex science into clear, submission-ready documents, we’d love to hear from you.
How you might spend your days
- Proactively preparing clinical and regulatory documents to support AbCellera’s clinical development programs, including Module 2 to 5 documents, briefing books, safety updates, and responses to regulatory agencies
- Organizing and conducting document review meetings, and partnering with project teams on authoring and content strategy
- Collaborating with team members to align on deliverables, writing processes, and timelines
- Staying current on US and international regulations and medical writing practices</
