Leverage your experience in medical writing as a Regulatory Medical Writer, responsible for crafting documentation for research initiatives. Collaborate with diverse stakeholders to ensure precision and compliance in regulatory submissions.

You will manage the development of key regulatory documents, utilizing your 3-5 years of relevant experience, and act as the primary liaison with publication specialists. Focusing on quality control and adherence to guidelines, you will support various teams in producing key research documents and presentations while ensuring timely completion.

Key Responsibilities:
• Coordinate and produce high-level regulatory documents
• Engage collaborators to refine specialized scientific content




• Provide project management for tracking progress and deliverables
• Lead quality reviews for external writing projects
• Assist study teams with editorial support on templates

Requirements:
• Undergraduate degree, advanced degrees preferred
• 3-5 years of experience in medical writing
• Trained in GCP, GDPR, and HIPAA standards
• Familiarity with EndNote/reference management software
• Robust written communication skills and attention to detail

Elevate your writing skills in this vital role and contribute to cutting-edge research.
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📌 Regulatory Medical Writer Role (Ontario)
🏢 Alimentiv 2
📍 Ontario