Drive clinical excellence as a full-time Research Coordinator I at St. Michael's Hospital, Toronto. This role focuses on clinical trials, regulatory compliance, and patient engagement.

As a Research Coordinator I in the Clinical Research Program, you will play a vital role managing clinical trials and data collection across various research teams. This position requires solid project coordination skills, emphasizing compliance with Good Clinical Practice and Health Canada regulations. You will also effectively recruit patients, guide study operations, and maintain communication with stakeholders throughout trial phases.

Key Responsibilities:
• Coordinate screening and recruitment of clinical trial participants
• Manage study-related documentation and data accuracy




• Facilitate meetings and communications with internal teams
• Support the ethical and regulatory submission process
• Ensure proper maintenance of study supplies and inventory

Requirements:
• Bachelor's Degree in Health Sciences or related field
• 2 years of clinical research experience preferred
• Familiarity with regulated clinical drug trials
• Strong organizational and problem-solving skills
• Experience in stakeholder communication and engagement

In this role, leverage your clinical knowledge and coordination skills to enhance research efficiency and patient care.
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📌 Clinical Research Coordinator Role in Toronto (Ontario)
🏢 St. Michael's Hospital
📍 Ontario