Description
The Clinical Research Coordinator will manage and coordinate clinical research studies in accordance with Good Clinical Practice, Health Canada, IRB, and ICH-GCP requirements. Responsibilities include participant recruitment and consent, scheduling, follow-up, data entry into electronic data capture systems, regulatory documentation, adverse-event reporting, and preparation for monitoring visits, audits, and inspections. The role is on-site in a physician practice and clinical research setting and may involve handling biological samples and working with patients.
