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

• 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 accordance with ICH-GCP, Health Canada, FDA, US Federal Code, and applicable institutional policies
• Support study management activities, including tracking milestones and deliverables
• Assist with clinical trial monitoring according...