Study Coordinators are essential members of the research team and are responsible for the support and conduct of the protocol specific activities at the Participating Organization. They oversee the protocol specific activities at that site including administrative, data management, and overall clinical and research support for Consortium investigators and their clinical trials. The resources below are made available to assist with the efforts required of the Study Coordinator.
Common Toxicity Criteria for Adverse Events and Deviation Reporting
• NCI/CTEP Common Terminology Criteria for Adverse Events (CTCAE) and Common toxicity Criteria (CTC)
• SAE Reporting Form
• SAE Instructions for Completion
• DCP Protocol Deviation Notification Form