Elevate your career as a Medical Writer, providing essential writing services to Clinical Research Scientists and Sponsors. Collaborate on regulatory documents and ensure compliance with industry standards in this dynamic position.

We are seeking an experienced Medical Writer with 3-5 years of relevant experience. You will coordinate the production of clinical regulatory documents including protocols and informed consent forms. Engage with both internal teams and external publication executives to drive project success and maintain timelines.

Key Responsibilities:
• Produce and edit regulatory documents for clinical research projects
• Manage writing timelines and deliverables effectively
• Liaise with external publication stakeholders for content revisions




• Conduct quality control reviews on documents from other authors
• Assist with writing or editing study-related materials as needed

Requirements:
• Undergraduate degree, advanced degree preferred
• 3-5 years of experience in medical writing
• Familiarity with GCP, GDPR, and HIPAA regulations
• Advanced knowledge of EndNote/reference software
• Robust communication skills, diplomacy, and tact

Leverage your medical writing expertise in supporting clinical research with high-quality documentation and communication.
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📌 Medical Writer for Clinical Research (Ontario)
🏢 Alimentiv
📍 Ontario