Clinical Trial Site Execution (Real-World Settings)
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This subcontract, titled Clinical Trial Site Execution (Real-World Settings), is issued by the National Institutes of Health under the Department of Health and Human Services. The selected provider will support prime contractors on NIMH and NIDA RAPIDs-CTN projects by performing patient recruitment and executing clinical trial protocols. The scope of work focuses on high-need populations, specifically those with acute suicide risk and treatment-resistant conditions, requiring the contractor to possess the clinical capacity to manage complex psychiatric patients. Operations will be conducted across various real-world environments, including Inpatient Psychiatric Units, VA Medical Centers, and Community Mental Health Centers. The primary deliverables for this engagement include the delivery of recruited patient cohorts and the submission of site-level protocol compliance reports. The opportunity is categorized under NAICS code 622310, with a response deadline set for June 10, 2027.
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Documents
This scope was carved out of RFA-MH-27-150.
The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.
Advancing Real-World Effectiveness Evidence for Rapid-Acting Psychotropic Interventional Drugs (RAPIDs) (UM1 Clinical Trial Required)
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This scope is part of a larger contract. Its documents live on the prime.
- 1 document on the prime contractFrom Advancing Real-World Effectiveness Evidence for Rapid-Acting Psychotropic Interventional Drugs (RAPIDs) (UM1 Clinical Trial Required)
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