Sr Medical Writer, Redaction (Clinical Trial Transparency)

Updated: April 29, 2026

Location: Toronto, ON, Canada

Job ID: -OTHLOC-1510-2DR

Sr Medical Writer, Redaction (Clinical Trial Transparency)

Job Responsibilities

• Execute project-specific activities with high quality and in defined timelines according to standard processes and operating procedures.
• Marking / QC / Review and/or editing of pertinent documents such as clinical study documents or any other documents for regulatory submission (clinical study reports, patient narratives, clinical summaries, etc. for different regulations such as EMA policy 0070, Health Canada PRCI, EUCTR regulation, final rule‑NIH).
• Protocol and results summaries to support clinical trial disclosure commitments.
• Systematically perform quality control checks of documents prepared by colleagues against pre‑specified checklists generated in ...