I currently work as a Clinical Research Coordinator in the Oncology Department. My role involves patient coordination, data entry and management, regulatory documentation, and overall clinical trial support. I have experience working with EDC systems, maintaining Investigator Site Files (ISF) and patient binders, ensuring ICH-GCP compliance, and coordinating with sponsors, CROs, study teams, and patients to keep trials running smoothly. I also have experience reviewing and coordinating Clinical Trial Agreements (CTAs), budgets, and other study-related contracts.
