Join Centricity Research in Toronto as a Clinical Research Coordinator where you will play a key role in managing clinical trials and ensuring participant compliance and safety.

At Centricity Research, we are seeking a skilled Clinical Research Coordinator for our new LMC Multispecialty site in Toronto. This full-time position demands independent coordination of clinical studies, including participant visits and conducting phlebotomy. The ideal candidate thrives in a team-oriented environment and is ready to contribute right away.

Key Responsibilities:
• Manage study visits in line with protocols and regulations
• Oversee participant safety and document all events accurately
• Execute clinical tasks including vitals and sample collection




• Implement recruitment strategies and facilitate consent documentation
• Maintain study compliance through regular quality checks

Requirements:
• Bachelor’s degree in relevant health or research field
• Minimum 3 years' experience in clinical research
• Qualification for phlebotomy in Canada
• Strong familiarity with medical and regulatory documentation
• Proactive, organized, and effective communicator

Make a significant impact in clinical research by prioritizing participant well-being and compliance at Centricity Research in Toronto.
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📌 Clinical Research Coordinator at Centricity Research (Ontario)
🏢 Centricity Research
📍 Ontario