Join a dynamic team as an Experienced Medical Writer, providing essential writing services for research projects. Your role will involve crafting regulatory documents and consulting with stakeholders, ensuring quality and compliance.

This position requires 3-5 years of experience in medical writing, ideally with a focus on protocols, informed consent forms, and clinical study reports. You will work closely with Clinical Research Scientists and external specialists to ensure documents align with industry standards. Additionally, you will track writing project timelines and aid in document quality control.

Key Responsibilities:
• Produce and manage regulatory documents with strict adherence to guidelines
• Collaborate with authors to refine and publish scientific content




• Act as project manager, tracking deliverables and timelines
• Participate in quality control reviews for external authors
• Support study teams in reviewing key documents as needed

Requirements:
• Bachelor’s degree, advanced degrees preferred
• 3-5 years of medical writing experience
• Knowledge of GCP, GDPR, and HIPAA guidelines
• Proficiency in EndNote/reference software
• Robust communication skills with a focus on diplomacy

Utilize your medical writing expertise to contribute to impactful research projects.
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📌 Experienced Medical Writer Opportunity (Ontario)
🏢 Alimentiv 2
📍 Ontario