Updated: May 7, 2026 | Location: Toronto, ON, Canada | Job ID:

Job Responsibilities

• Leads the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately.
• Manages medical writing activities associated with individual studies, coordinating activities within and across departments with minimal supervision.
• Completes a variety of documents, including clinical study protocols, clinical study reports, patient narratives, annual reports, investigator brochures, informed consents, plain language summaries, periodic safety update reports, clinical development plans, IND submissions, integrated summary reports, NDA and eCTD submissions, journal manuscripts, abstracts, posters, and presentations for scientific meetings.
• Adheres to established regulatory standards (e.g., ICH E3 guidelines) and company SOPs, client standards, and approved temp...