Elevate your clinical research career at Sunnybrook Research Institute as a Clinical Research Assistant. This in office role is pivotal for managing multiple clinical trials and enhancing patient research access.
The Clinical Research Assistant will work at the Centre for Clinical Trial Support, closely assisting interdisciplinary teams and Principal Investigators in various trial activities. Your responsibilities will include trial coordination, participant management, compliance monitoring, and supporting operational tasks tailored to strengthen clinical research at SRI.
Key Responsibilities:
• Facilitate and manage clinical trial operations effectively
• Handle participant screening, data management, and consent
• Coordinate submissions to Ethics Board and manage legal contracts




• Liaise with hospital departments for study approvals
• Schedule patient follow-up visits ensuring protocol adherence
Requirements:
• Minimum 2 years of clinical research experience
• Bachelor’s degree in a health-related discipline
• Understanding of research ethics and regulations (ICH/GCP)
• Proficient with Microsoft Office and data systems
• Solid communication skills and ability to work independently
Support groundbreaking clinical research at Sunnybrook and enhance patient care through your role.
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📌 Clinical Trials Coordinator At Sunnybrook Institute Toronto
🏢 Sunnybrook
📍 Toronto