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Job Description & How to Apply Below
At Toronto Western Hospital, the Clinical Research Analyst will assist in the execution of clinical trials under various principal investigators. Key responsibilities include preparing and maintaining research ethics board applications and supporting participant recruitment by screening potential subjects. This role involves data collection, adhering to ICH/GCP guidelines, and ensuring the integrity of regulatory documents.
Key Responsibilities:
• Assist with Research Ethics Board applications and approvals
• Coordinate study participant recruitment and informed consent
• Maintain source documentation and data entry accuracy
• Handle administrative tasks related to study management
• Conduct interviews and assist with trial visits
Requirements:
• Bachelor’s degree in a health/science discipline
• 1-2 years of clinical trial research experience
• Knowledge of ICH-GCP and Health Canada regulations
• Familiarity with electronic data capture systems
• Strong communication and organizational skills
Make a significant impact on clinical trials and contribute to cutting-edge research at UHN in Toronto.
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