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.

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