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 robust project coordination skills, emphasizing compliance with Positive 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
Robust 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.

📌 Clinical Research Coordinator Role In Toronto
🏢 St. Michael's Hospital
📍 Toronto