Coordinate clinical research studies in office using GCP knowledge, EDC systems, and accurate participant management in clinical settings.

This Clinical Research Coordinator manages study activities with investigators, sponsors, and participants. The work supports protocol integrity, accurate data collection, and regulatory compliance. Key skills include participant coordination, Health Canada requirements, and electronic data capture.

Key Responsibilities:
Coordinate recruitment, consent, scheduling, and participant follow-up
Conduct clinical research studies according to approved protocols
Enter accurate data into electronic data capture systems
Maintain regulatory binders, subject files, and case report forms




Monitor adverse events and communicate with sponsors and IRB

Requirements:
Bachelor’s degree in health, life sciences, nursing, or related field
One to three years of clinical research experience preferred
Knowledge of GCP, Health Canada, and IRB regulations
Phlebotomy certification and IATA-compliant sample processing proficiency
Proficiency with Medidata, RAVE, and Microsoft Office Suite

Apply clinical research coordination, regulatory knowledge, phlebotomy, and EDC skills across in office physician practice studies.
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📌 Clinical Research Study Coordinator Hamilton (Canada)
🏢 ClinSurge
📍 Canada