Clinical Research Coordinator I

Union: Non-Union
Number of vacancies: 1
New or Replacement Position: New
Site: Rumsey Centre (347 Rumsey Road, Toronto), Toronto Rehab  
Department: Cardiovascular Prevention and Rehabilitation Program
Reports to: Senior Manager, Clinical Research Services 
Salary Range: $37.47 - $46.84 per hour
Hours: 37.5 hours per week
Shifts: 5 days per week
Status: Temporary Full-time (1 year)
Closing Date: March 19, 2026

Position Summary
The CorPath Study offers an exciting opportunity for a highly organized, motivated, and results-driven Clinical Research Coordinator I seeking a dynamic and challenging role. The ideal candidate is detail-oriented, adaptable, and comfortable working independently in a fast-paced research environment.

Applicants should have familiarity with cardiovascular disease, medical terminology. This role requires both precision and initiative, with responsibilities ranging from data management to participant screening and recruitment. As study priorities may evolve in response to funding agency requirements, the successful candidate must demonstrate flexibility and the ability to adapt to changing operational needs.

Duties
The Clinical Research Coordinator I will work closely with the study team to:

• Screen, enroll, and follow participants through the informed consent process
• Obtain medical histories and ensure protocol-specific testing is scheduled and completed
• Prepare and maintain research files, complete case report forms, and document adverse events
• Plan, implement, and coordinate data entry activities with a focus on accuracy and compliance
• Provide recruitment and progress updates to study sponsors, including milestones toward enrollment targets
• Actively support recruitment efforts, including in-services, development of marketing materials, and preparation of stakeholder reports
• Monitor participant health status changes, triage concerns to the Study Physician as appropriate, and document findings
• Conduct pre–coronary computed tomography angiography (CCTA) screening and triage to the Study Physician as required
• Collaborate with the JDMI team to coordinate bookings related to study-initiated CCTA appointments
• Perform cross-functional duties consistent with the job classification as assigned