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 professionals 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 on-site
• 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 (Ontario)
🏢 University Health Network
📍 Ontario