Join Centricity Research as a Clinical Research Coordinator in Vaughan. Utilize your medical expertise in participant visits, phlebotomy, and regulatory compliance every day.
We are looking for an experienced Clinical Research Coordinator to oversee clinical studies at our Vaughan site. This position involves independent study coordination, maintaining participant safety, and effectively collaborating with team members. Your role will ensure compliance with protocols and regulatory requirements, contributing to the success of our clinical trials.
Key Responsibilities:
• Conduct study visits per protocols and regulations
• Ensure participant well-being by reporting adverse events
• Perform vitals, ECGs, and sample collection




• Support recruitment of eligible study participants
• Accurately document study data for audits and monitoring
Requirements:
• Bachelor’s degree in a relevant field or equivalent experience
• Minimum 3 years of clinical research experience
• At least 3 years of phlebotomy experience in Canada
• Robust knowledge of medical terminology and GCP
• Detail-oriented with organizational skills
Contribute your research expertise and commitment to quality at Centricity Research in Vaughan today.
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📌 Clinical Research Coordinator In Vaughan (Canada)
🏢 Centricity Research
📍 Canada