Coordinate gastrointestinal and liver clinical trials at the University of Alberta, using participant management and study coordination expertise. This regular full time Research I role works days at U of A Hospital.
Assigned to the Gastrointestinal and Liver Disease Research Group, you will support Investigators in pharmaceutical clinical research. Responsibilities include recruitment, informed consent, patient care, protocol assessments, scheduling, documentation, and compliance monitoring. You will also educate participants and maintain training records.
Key Responsibilities: Screen, recruit, enroll, and retain study participants
Obtain informed consent and provide participant education
Complete protocol assessments and schedule procedures




Prepare source documents and maintain study records
Monitor compliance and review laboratory and diagnostic reports
Requirements: Diploma or degree in health or science
Four to five years of pharmaceutical clinical research experience
Hepatology and Gastroenterology Phase I–IV trial experience
Knowledge of ICH-GCP, Health Canada, and FDA requirements
Proficiency with EDC systems, iMedidata, Connect Care, and Netcare
Apply clinical trial coordination, participant management, and regulatory knowledge within GILDR’s gastrointestinal and liver research program.

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📌 Clinical Trials Research Coordinator (Alberta)
🏢 Alberta Health Services
📍 Alberta