Elevate your research career with Centricity Research as a Clinical Research Coordinator in Vaughan. Focus on participant safety and efficient study management practices.

We seek a full-time Clinical Research Coordinator to independently conduct clinical studies at our Vaughan Endocrinology site. This role will have a significant impact on participant engagement and data integrity while ensuring compliance with clinical study protocols. Work closely with Investigators and enhance your skills in various therapeutic areas.

Key Responsibilities:
• Coordinate study visits using established protocols
• Monitor participant safety and document adverse events
• Perform clinical tasks including vitals and ECGs
• Assist in participant enrollment and informed consent
• Prepare documentation for audits and inspections

Requirements:
• Bachelor’s degree in health or research-related field
• 3+ years of hands-on clinical research experience
• Current phlebotomy qualifications in Canada
• Proficient in GCP and clinical documentation
• Robust organizational and multitasking abilities

Bring your dedication and detail-oriented approach to Centricity Research in Vaughan.
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📌 Experienced Clinical Research Coordinator (Ontario)
🏢 Centricity Research
📍 Ontario