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.

📌 Remote Scientific Medical Writer GTA (Calgary)
🏢 Intrahealth
📍 Calgary