Location
, , canada
Job Type
Full-time
Posted
June 11, 2026
Job Description
Elevate your medical writing career with ProPharma as a Senior Medical Writer in Canada. This role requires expertise in regulatory documents and clinical research, offering a hybrid work model.
With over 25 years of dedication to patient wellness, ProPharma is seeking a Principal Medical Writer to manage clinical and regulatory documents, including protocols and study reports. This full-time position emphasizes high-quality deliverables, effective communication, and mentorship of less experienced writers, all while adhering to strict regulatory standards.
Key Responsibilities:
• Author clinical and regulatory documents independently
• Manage timelines and client expectations for projects
• Coordinate cross-functional teams for deliverables
• Conduct peer reviews and maintain quality control
• Lead departmental initiatives to enhance processes
Requirements:
• Bachelor’s degree in medical or scientific discipline
• Minimum 7 years of medical writing experie...
With over 25 years of dedication to patient wellness, ProPharma is seeking a Principal Medical Writer to manage clinical and regulatory documents, including protocols and study reports. This full-time position emphasizes high-quality deliverables, effective communication, and mentorship of less experienced writers, all while adhering to strict regulatory standards.
Key Responsibilities:
• Author clinical and regulatory documents independently
• Manage timelines and client expectations for projects
• Coordinate cross-functional teams for deliverables
• Conduct peer reviews and maintain quality control
• Lead departmental initiatives to enhance processes
Requirements:
• Bachelor’s degree in medical or scientific discipline
• Minimum 7 years of medical writing experie...
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