- Remote, Canada
- Remote
- Full-time · Principal
As a Principal Medical Writer, you'll play a critical role in developing high-quality clinical and regulatory documents that support drug development programs. Beyond writing, you'll have opportunities to lead projects, build strong client relationships, mentor colleagues, and help shape best practices across our Medical Writing organization.
Responsibilities
- Research, develop, write, and edit high-quality clinical and regulatory documents
- Lead complex medical writing projects, ensuring scientific accuracy, regulatory compliance, and timely delivery
- Prepare key clinical documents, including Clinical Study Reports (CSRs), Investigator's Brochures (IBs), and Informed Consent Forms (ICFs)
- Serve as a lead medical writer, submission coordinator, and primary client contact, as appropriate
- Coordinate contributions from multiple writers and cross-functional stakeholders
Requirements
- Bachelor's degree in Life Sciences, Health Sciences, or a related discipline, or equivalent qualifications