Guide clinical research operations at CHEO RI using regulatory expertise, GCP knowledge, and strong study start-up support in a hybrid model.
The Research Navigator supports CHEO RI researchers and teams across complex clinical research processes. This temporary full-time, 15-month position covers study activation, Research Ethics Board submissions, Health Canada requirements, research agreements, budgets, and clinical trial operations. Reporting to the Director, Research Operations, the role also supports the Clinical Trials Access Core and Clinical Investigation Unit. You will contribute to RareKids-CAN, operational metrics, process improvement, and strategic projects.
Key Responsibilities: Guide researchers through study start-up and institutional processes
Support REB, Health Canada, and research agreement requirements




Review clinical trial applications and essential documents
Facilitate compliant clinical research operations with internal partners
Develop guidance documents, workflows, and educational resources
Requirements: Bachelor’s degree in health sciences or related field
Minimum five years as a Research Coordinator
Knowledge of investigator-initiated and industry-sponsored clinical trials
Exceptional GCP and regulated clinical research knowledge
Solid Microsoft 365, communication, and organizational skills
Bring clinical trial management, regulatory guidance, and operational coordination expertise to CHEO RI’s research community in Ottawa.

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📌 Research Navigator Clinical Trials (Quebec City)
🏢 CHEO
📍 Quebec City