Job Description Summary:  Salary Range: $60,000–$80,000 per year 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 master file management. Ensure trials are conducted in acc...