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.

📌 Clinical Research Assistant Toronto
🏢 Universityhealthnetwork
📍 Toronto