Job Description Summary

Hours: 35 hours/week; 8:00 am - 4:00 pm Monday-Friday

Status: Full Time

Level: 2 Years Experience

Education & Qualifications

• At minimum, completion of a Bachelor of Science degree or recognized equivalent
• Fluency in French is an asset.

Duties & Responsibilities

The Clinical Research Associate (Clinical Data & Regulatory Affairs Specialist) supports the development, coordination, and oversight of CMRG-sponsored clinical research from protocol development through activation, follow-up, and close-out. Key responsibilities include but are not limited to:

• Contribute to protocol development, drafting, and amendments
• Coordinate study activities across single- and multicentre trials to support timelines and deliverables
• Support regulatory compliance, including Health Canada submissions (e.g., CTA/NOL), amendments, reporting, documentation and trial mas...