PROTOCOL INFORMATION OFFICE (PIO) SUPPORT SERVICES FOR THE PROCESSING OF CLINICAL TRIAL PROTOCOL DOCUMENTS AND TRACKING THE IMPLEMENTATION AND COMPLETION OF HUMAN CLINICAL RESEARCH STUDIES. PERFORMANC

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The major objective of this requirement is to provide support, which is defined by the five project areas detailed below, to the NCI, DCP Protocol Information Office (PIO). The five project areas are: Project Area 1. Abstraction of Key Elements from Protocol Related Documents Project Area 2. File Management Project Area 3. Clinical Trial Review Support Project Area 4. Manage People (persons such as investigators, coordinators, reviewers. etc.) and Organization’s data in DCP Clinical Trials Database Project Area 5. PIO Operational Support