Support oncology research data at Princess Margaret Cancer Centre using clinical record review, electronic case report forms, and Microsoft Excel.This temporary full time Clinical Study and Regulatory Assistant supports UHN's Cancer Genomics Program and a large-scale Molecular Residual Disease study. The position focuses on accurate clinical data curation, regulatory documentation, and study coordination. You will collaborate with clinical and biospecimen management teams while applying protocols, privacy requirements,



and applicable regulations.Key Responsibilities:Extract and validate clinical information from medical recordsEnter study data into electronic case report formsReview data quality and resolve discrepancies with study teamsMaintain trackers and longitudinal participant follow-up recordsAssist with Research Ethics Board submissions and amendmentsRequirements:Community college diploma in a health-related discipline requiredThree to six months of related experience requiredClinical research experience and knowledge preferredHigh proficiency in Microsoft ExcelOncology, clinical trials, or medical terminology experienceApply clinical research knowledge, careful data review, and regulatory coordination skills within UHN's Cancer Genomics Program.

📌 Clinical Research Data Assistant (Toronto)
🏢 University Health Network
📍 Toronto