Advance your expertise with Centricity Research as a Clinical Research Coordinator. This Toronto position involves participant management and regulatory compliance in clinical trials.

Centricity Research is expanding its Toronto LMC Multispecialty team by hiring a full time Clinical Research Coordinator. You will independently manage clinical studies, conduct visits and phlebotomy, ensuring all activities comply with applicable protocols. The role is ideal for someone who can manage multiple responsibilities while maintaining a keen eye for detail.

Key Responsibilities:
• Independently coordinate clinical studies ensuring compliance
• Conduct participant visits and monitor safety thoroughly
• Handle clinical procedures, including ECGs and sample processing




• Drive recruitment strategies and manage participant interactions
• Prepare documentation and oversee quality control checks

Requirements:
• Bachelor's degree in health or science field
• At least 3 years of clinical research experience
• Qualified to perform phlebotomy in Canada
• Extensive knowledge of regulatory compliance
• Self-motivated and detail-oriented

Take the lead on coordinating impactful clinical research studies that prioritize participant safety at Centricity Research in Toronto.
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📌 Experienced Clinical Research Coordinator Role (Ontario)
🏢 Centricity Research
📍 Ontario