Elevate your career as an Experienced Medical Writer, focusing on regulatory documentation and publication support for Clinical Research and academic partners. This role offers opportunities to craft impactful scientific content.

We seek a detail-oriented Medical Writer with 3-5 years of relevant experience. In this position, you will produce vital documents like protocols and informed consent forms while ensuring compliance with regulatory standards. You’ll also coordinate project timelines and quality control.

Key Responsibilities:
• Produce and manage regulatory documents consistent with guidelines
• Work with technical specialists to finalize publication content
• Track progress and report timelines to stakeholders




• Participate in quality control of peer-written documents
• Assist writing or reviewing training materials as needed

Requirements:
• Minimum undergraduate degree required; advanced degree preferred
• Prior experience in medical writing, especially clinical protocols
• Understanding of GCP, GDPR, and HIPAA standards
• Proficiency in EndNote and graphical software is beneficial
• A mindset focused on continuous improvement and learning

Capitalize on your medical writing expertise to support vital publications and enhance research outcomes.
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📌 Experienced Medical Writer Role (Quebec City)
🏢 Alimentiv
📍 Quebec City