Become a Clinical Research Coordinator in Toronto, managing clinical studies with a focus on integrity and compliance with Positive Clinical Practice. Engage with investigators, participants, and sponsors in an on-site role.

This position requires a detail-oriented individual to oversee clinical research studies following institutional guidelines and federal regulations. Key responsibilities include recruiting participants, collecting data, and ensuring adherence to study protocols. Experience in clinical research is preferred, with strong organizational and communication skills necessary for successful study management.

Key Responsibilities:
• Coordinate participant recruitment, consent, and follow-up
• Ensure compliance with GCP and regulatory requirements




• Collect and accurately input data into EDC systems
• Maintain study documents and regulatory binders
• Collaborate with teams including investigators and sponsors

Requirements:
• Bachelor’s degree in health or life sciences
• 1-3 years of clinical research experience preferred
• CCRC or CCRP certification is a plus
• Phlebotomy certification and proficiency required
• Strong knowledge of Health Canada and GCP regulations

Apply your expertise in clinical research coordination while ensuring high standards of data integrity.
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📌 Clinical Research Coordinator Position Toronto (Ontario)
🏢 ClinSurge Research
📍 Ontario