ICON plc, a world-leading healthcare intelligence and clinical research organisation, is seeking a Clinical Research Associate (CRA) to monitor clinical studies at investigative sites or remotely. You will ensure trials are conducted, recorded, and reported in accordance with the protocol, SOPs, ICH-GCP, and regulatory requirements. The role requires a bachelor’s degree in a scientific or health-related field, 1+ years of monitoring experience for level 2 (3+ for level 3), and oncology
📌 Clinical Research Associate: Trial Monitoring (Winnipeg)
🏢 GL
📍 Winnipeg