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 participantsPerform delegated study-specific assessments and participant follow-upSchedule visits, laboratory work,



and study proceduresMaintain audit-ready regulatory and study documentationCoordinate sponsors, monitors, and hospital departmentsRequirements:Undergraduate degree or relevant clinical research experienceAt least six months coordinating trials or research studiesWorking knowledge of ICH GCP, NIH, and ethics requirementsMicrosoft Office, Google Workspace, and CTMS proficiencyValid Alberta Class 5 driver’s licence and own transportationApply clinical research coordination, participant communication, protocol management, and documentation skills across concurrent studies in Edmonton.#J-18808-Ljbffr

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