This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Research Associate based in Canada.

This role offers the opportunity to contribute directly to the successful delivery of clinical research studies from site start-up through closeout.
You will monitor clinical sites across Phase I to III studies, ensuring protocol adherence, data quality, and participant safety.
Working closely with investigators, site personnel, and cross-functional teams, you’ll help resolve issues and keep studies on track.
The position combines scientific expertise, regulatory knowledge, relationship management, and hands-on site monitoring.
You’ll play an important role in maintaining compliance with GCP, ICH guidelines, applicable regulations, and study-specific requirements.
This is a dynamic environment suited to an organized and analytical professional who can manage competing priorities independently.
With significant travel, the role provides broad exposure to clinical research operations and meaningful opportunities to influence study quality.

What the job really is