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.
Experience: 2 - 5 years
Experience: 6 months - 1 year
Experience: 1 - 2 years
Experience: 1 - 2 years
Experience: 1 - 2 years
Experience: Less than 6 months
Experience: Less than 6 months
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