This Scope of Work outlines work that will be performed by study site over and above work that is already covered under the original Scope of Work for the site’s participation as a performance site in the C-TRACT Clinical Trial. Study site agrees to commit additional time from research coordinator to the following tasks, in collaboration with hematology co-investigators, and with oversight from Dr. Kush Desai: (1) routine pre-screening of clinic patient lists from the interventional radiology and hematology services, with subsequent communication with Dr. Desai and other physician co-investigators; (2) submission of a written summary that delineates the specific work activity completed to the C-TRACT clinical coordinating center (CCC) on a monthly basis; and (3) participation in dedicated monthly teleconferences with the C-TRACT clinical coordinating center (CCC), other study leaders, and personnel from other study sites. Funding Element: 5 hours/week effort for Kristie Kennedy (clinical research coordinator)
|Effective start/end date||9/1/21 → 8/31/23|
- Washington University St. Louis (WU-23-0360//5UH3HL138325-05)
- National Heart, Lung, and Blood Institute (WU-23-0360//5UH3HL138325-05)
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