Turn clinical findings into transparent, accurate documentation as a fully remote Senior Medical Writer with dicentra in Ontario. Apply rigorous scientific writing. This senior medical writing opportunity supports studies across pharmaceuticals, medical devices, and natural health products. You will develop protocols, informed consent forms, Investigator’s Brochures, and Clinical Study Reports. Collaboration spans clinical operations, biostatistics, data management, regulatory specialists, and sponsors.

Key Responsibilities
- Integrate clinical findings, safety data, and scientific interpretation
- Conduct literature reviews and synthesize scientific evidence
- Review documents for accuracy, consistency, and completeness
- Apply ICH-GCP principles, SOPs, and sponsor requirements




- Collaborate with clinical research and regulatory professionals

Requirements:
- Degree in life sciences, health sciences, pharmacy, or related discipline
- Advanced degree preferred, including Master’s, Pharm.
D., or Ph.
D.
- Five or more years writing medical or regulatory documents
- Exceptional technical writing, editing, and critical review skills
- Ability to work independently with minimal supervision Use medical writing, clinical research knowledge, and scientific interpretation skills to strengthen dicentra’s trial documentation remotely.

📌 Senior Medical Writer Clinical Trials (Canada)
🏢 dicentra
📍 Canada