Explore a Clinical Medical Writer chance where your writing skills will directly support Clinical Research teams and academic institutions. Focus on producing regulatory documents while maintaining high-quality standards.

This role requires a Medical Writer with a minimum of 3-5 years in medical writing, capable of producing essential documents like clinical study reports and protocols. Engage in project management and stakeholder communication to ensure timely delivery and regulatory compliance.

Key Responsibilities:
• Lead the development of regulatory and publication documents
• Collaborate with various authors to refine content
• Manage timelines and report progress regularly
• Support quality reviews of documents authored by peers




• Act as a liaison with publication specialists

Requirements:
• Undergraduate degree in a relevant discipline; advanced degree preferred
• 3-5 years of experience in medical writing
• Experience with GCP, GDPR, and HIPAA regulations
• Advanced knowledge of reference management software
• Familiarity with prior knowledge in Gastroenterology preferred

Utilize your skills to make a significant impact in clinical research documentation and collaboration.
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📌 Clinical Medical Writer Opportunity (Quebec City)
🏢 Alimentiv
📍 Quebec City