Join our team as a Medical Writer, providing essential writing services for Clinical Research Scientists and academic partners. This role focuses on crafting regulatory documents and requires solid communication skills.

We are looking for an experienced Medical Writer with a minimum of 3-5 years in the field. You’ll engage in producing protocols, clinical study reports, and informed consent forms. Your expertise will ensure alignment with industry standards while efficiently managing writing projects and timelines.

Key Responsibilities:
• Lead the planning and creation of regulatory documents
• Coordinate with authors and specialists for content completion
• Manage writing deliverables and track project timelines




• Review and critique documents authored by others
• Serve as liaison with external publication executives

Requirements:
• Undergraduate degree in a relevant field, advanced degree preferred
• 3-5 years of medical writing experience
• Familiarity with GCP, GDPR, and HIPAA regulations
• Proficient in EndNote/reference software
• Knowledge of Gastroenterology is an asset

Leverage your writing skills and industry knowledge to contribute to impactful clinical research documentation.
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📌 Medical Writer for Clinical Research (Quebec City)
🏢 Alimentiv
📍 Quebec City