Join Pharma Medica Research as an Associate Medical Writer in Mississauga. This role focuses on producing high-quality clinical documentation for Phase I to III studies.
At Pharma Medica, we value cutting-edge professionals who are eager to learn and grow. As an Associate Medical Writer, you will be responsible for drafting essential sections of Clinical Study Reports (CSRs) based on study interpretations. Additionally, you'll have the chance to review clinical documentation, engage in protocol development, and enhance your knowledge of regulatory requirements.
Key Responsibilities:
• Draft conclusions for CSRs and relevant documents
• Collaborate on eCRF design and review outputs
• Respond to sponsor comments effectively




• Prepare clinical protocol documentation as needed
• Conduct literature reviews on selected topics
Requirements:
• BSc in Medical Sciences or a related field
• One year experience in medical writing within a CRO
• Familiarity with ICH and GCP regulations
• Solid writing and editorial capabilities
• Robust communication and teamwork skills
Shape your career in medical writing at Pharma Medica Research while delivering vital documentation that ensures clinical trial success.
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📌 Associate Medical Writer Opportunity Mississauga (Canada)
🏢 Pharma Medica Research
📍 Canada