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 UHNs 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 UHNs Cancer Genomics Program.