Advance your writing career with a full time Scientific Medical Writer role focused on Phase 1-IV studies, remote from the Greater Toronto Area. Contribute to essential documents while ensuring compliance and quality throughout.

We are seeking a Scientific Medical Writer 1 to join our remote team. This position requires at least three years of experience in scientific protocol design and writing, particularly in the context of Phase I and bioequivalence studies. You will interact with scientists and regulatory agencies, ensuring that all documents meet Good Clinical Practice (GCP) standards.

Key Responsibilities:
• Write protocols and consent forms for studies
• Conduct literature searches and NDA reviews
• Collaborate with PK Scientists and Biostatisticians




• Prepare for interactions with Institutional Review Boards
• Ensure compliance with GCP and other guidelines

Requirements:
• PhD in Pharmacy, Pharmacology, or Life Sciences
• Minimum three years of scientific writing experience
• Experience in a CRO environment preferred
• Strong interpersonal and communication skills
• Attention to detail under tight timelines

Bring your expertise in scientific writing and protocol design to enhance our clinical studies remotely.
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📌 Remote Scientific Medical Writer GTA (New Brunswick)
🏢 Intrahealth
📍 New Brunswick