Coordinate clinical trials in person at North Campus, Edmonton, using participant management, protocol compliance, and research documentation skills.

The Clinical Research Coordinator supports clinical trials and investigator-initiated studies under the Principal Investigator. You will recruit, consent, and screen participants, conduct delegated assessments, manage follow-up, and coordinate study visits. The work requires careful adherence to ICH GCP, NIH guidelines, approved protocols, and institutional policies.

Key Responsibilities:

- Recruit, consent, and screen potential study participants
- Perform delegated study-specific assessments and participant follow-up
- Schedule visits, laboratory work, and study procedures
- Maintain audit-ready regulatory and study documentation




- Coordinate sponsors, monitors, and hospital departments

Requirements:

- Undergraduate degree or relevant clinical research experience
- At least six months coordinating trials or research studies
- Working knowledge of ICH GCP, NIH, and ethics requirements
- Microsoft Office, Google Workspace, and CTMS proficiency
- Valid Alberta Class 5 driver’s licence and own transportation

Apply clinical research coordination, participant communication, protocol management, and documentation skills across concurrent studies in Edmonton.

📌 Clinical Research Coordinator Edmonton (Canada)
🏢 Avenue.io
📍 Canada