Advance your career with UHN as a Clinical Study and Regulatory Assistant at the Princess Margaret Cancer Centre. This full time position focuses on regulatory compliance and clinical documentation support.
Join the Cancer Genomics Program team to facilitate personalized cancer medicine research. As a Clinical Study and Regulatory Assistant, you will prepare vital research ethics submissions, curate clinical data, and manage consent forms. Collaborate with experienced specialists while ensuring adherence to stringent research protocols.
Key Responsibilities:
• Prepare submissions for Research Ethics Board and CAPCR approvals
• Review and create essential study documents
• Curate clinical data into electronic case report forms (eCRFs)




• Collect genomic study consent forms in office
• Attend program and study meetings actively
Requirements:
• College diploma in a health-related discipline required
• 3 to 6 months related experience preferred
• Familiarity with oncology and clinical trials
• Excellent communication and organizational skills
• High proficiency in Microsoft Excel
Bring your passion for clinical research and compliance to UHN's cutting-edge Cancer Genomics Program.
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📌 Clinical Research Assistant At Uhn Toronto (Canada)
🏢 University Health Network
📍 Canada