Teams at Associated Urological Specialists

Supports clinical trials by completing study training, collecting patient vitals and biological samples, maintaining source documents and essential study records, entering case report forms, resolving queries, managing investigational products, maintaining supplies, administering questionnaires, coordinating visits, and scheduling scans. The role requires compliance with GCP, IATA, CPR, HIPAA, and applicable regulations while providing compassionate patient support in a hybrid healthcare research setting.