Coordinate clinical research studies on-site using GCP knowledge, EDC systems, and precise 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 on-site physician practice studies.
