Support breast surgical oncology research at Toronto General Hospital through participant communication, informed consent, and accurate study data collection. Work days, 35 hours weekly, temporarily.
As a Clinical Research Study Assistant, you will support the ABODE study portfolio under the Principal Investigator and research manager. Coordinate study activities, interact with participants, collect questionnaires and chart data, and maintain regulatory documentation. Follow approved protocols, UHN policies, and Valuable Clinical Practice guidelines.
Key Responsibilities: Screen and recruit participants for clinical research studies
Schedule virtual visits and maintain participant communication
Conduct informed consent with research participants
Collect questionnaires, chart reviews,



and eHealth platform data
Track surveys, adverse events, and protocol deviations
Requirements: Community college diploma in a health-related discipline or equivalent
Three to six months of related experience
Clinical research experience and research setting training preferred
Knowledge of GCP, research ethics, and study data handling
Microsoft Office proficiency; REDCap experience preferred
Apply clinical research coordination, participant communication, and data collection skills within UHN’s ABODE study portfolio in Toronto.

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📌 Clinical Research Assistant Toronto (Ontario)
🏢 Universityhealthnetwork
📍 Ontario