Join our team as a Clinical Research Coordinator to manage on-site clinical studies. You'll coordinate participant interactions, data management, and adherence to regulations in this essential role.
In this position, the Clinical Research Coordinator plays a pivotal role in executing clinical trials in line with Good Clinical Practice (GCP). You will collaborate closely with physicians, sponsors, and research teams to ensure rigorous compliance and accurate data collection throughout the research lifecycle.
Key Responsibilities:
• Oversee recruitment and scheduling of study participants
• Ensure adherence to Health Canada and IRB compliance standards
• Input collected data into electronic data capture systems accurately




• Maintain electronic regulatory binders and subject files
• Communicate adverse events to IRB and sponsors as required
Requirements:
• Bachelor’s degree in a relevant health science field
• Preferably 1-3 years of experience in clinical research
• Certified Clinical Research Coordinator is advantageous
• Phlebotomy certification and skills required
• Solid knowledge of regulatory practices and EDC systems
Leverage your research skills to contribute to critical clinical projects in our medical setting.
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📌 On-Site Clinical Research Coordinator Role (Hamilton)
🏢 Search Influence
📍 Hamilton