Senior Medical Writer

Responsibilities

• Prepare clinical and regulatory documents supporting clinical development programs, including Module 2 to 5 documents, briefing books, safety updates, and regulatory responses

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

• Align with team members on deliverables, writing processes, and timelines

• Stay current on US and international regulations and medical writing practices

• Lead adoption of AI-assisted writing tools to accelerate document preparation

• Build therapeutic area and product expertise across development programs

Requirements

• 8+ years of medical writing experience in pharma or biotech

• Relevant post-secondary degree

• Extensive experience writing clinical and regulatory documents per ICH, GCP and regulatory requirements

• Strong oral and written communication of complex scientific concepts

• Ability to manage multiple projects and collaborate cross-functionally

• Advanced understanding of drug development, clinical research, study design, biostatistics, pharmacology and medical terminology

Preferred Qualifications

• Experience preparing dossiers for biologic therapies

Benefits

• Hiring range CAD $118,000 - $150,000 annually plus equity and annual bonus

• 6% non-match RRSP contribution

• CAD $1,500 annual Active Lifestyle Allowance

• Annual vacation, professional development and comprehensive health benefits

About the Company

• AbCellera is a clinical-stage biotechnology company developing antibody-based medicines in endocrinology, women's health, immunology and oncology.