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 Positive Clinical Practice guidelines.Key Responsibilities:Screen and recruit participants for clinical research studiesSchedule virtual visits and maintain participant communicationConduct informed consent with research participantsCollect questionnaires, chart reviews,



and eHealth platform dataTrack surveys, adverse events, and protocol deviationsRequirements:Community college diploma in a health-related discipline or equivalentThree to six months of related experienceClinical research experience and research setting training preferredKnowledge of GCP, research ethics, and study data handlingMicrosoft Office proficiency; REDCap experience preferredApply clinical research coordination, participant communication, and data collection skills within UHN's ABODE study portfolio in Toronto.

📌 Clinical Research Assistant Toronto
🏢 Universityhealthnetwork
📍 Toronto