Coordinate stroke research studies at Sunnybrook Research Institute using clinical trial administration, participant recruitment, and data management skills on site.
This experienced Clinical Research Coordinator supports ongoing and upcoming studies within the Sunnybrook Stroke Research Unit. Coordinate investigator-initiated and industry-sponsored research, including Health Canada-regulated clinical trials. Work with investigators and study teams while following protocols, hospital policies, and ICH/GCP guidelines.
Key Responsibilities: Coordinate multiple research studies and clinical trials
Recruit, consent, enrol, and follow up study participants
Collect data and maintain study documentation
Schedule visits and coordinate participant appointments




Manage Research Ethics Board and contract submissions
Requirements: Bachelor’s degree in a health services-related discipline
Minimum three years of clinical research experience
Experience recruiting participants into multiple studies
Robust communication, organization, and problem-solving skills
Proficiency with Microsoft Office and study data platforms
Apply clinical research coordination, recruitment, documentation, and communication expertise within Sunnybrook’s Stroke Research Unit on site.

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📌 Clinical Research Coordinator Stroke Studies (Ontario)
🏢 Sunnybrook Health Sciences Centre
📍 Ontario