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 records
Enter study data into electronic case report forms
Review data quality and resolve discrepancies with study teams




Maintain trackers and longitudinal participant follow-up records
Assist with Research Ethics Board submissions and amendments
Requirements: Community college diploma in a health-related discipline required
Three to six months of related experience required
Clinical research experience and knowledge preferred
High proficiency in Microsoft Excel
Oncology, clinical trials, or medical terminology experience
Apply clinical research knowledge, careful data review, and regulatory coordination skills within UHN's Cancer Genomics Program.

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