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Clinical Research Coordination & Patient Recruitment

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This subcontract for Clinical Research Coordination and Patient Recruitment supports prime contractors on FY26 Spinal Cord Injury Research Program projects for the Department of the Army. The primary scope involves the recruitment and retention of study participants, the administration of pilot clinical trials, and the management of participant screening based on specific inclusion and exclusion criteria. To execute these tasks, the provider will utilize decentralized clinical trial tools and patient recruitment databases. The contract requires strict adherence to regulatory standards, including mandatory IRB approval and GCP certification. Key deliverables include the successful recruitment of the study population and the submission of detailed retention reports. The solicitation was posted on May 5, 2026, with a response deadline of November 12, 2026, under NAICS code 514199.

General Info

Army subcontract for spinal cord injury research coordination, patient recruitment, and trial management.

Agency

Department Of Defense → Department Of The Army -- UsamraaView Agency

NAICS

514199 - NAICS Code 514199

Place of Performance

Not specified

Set-Aside

NONE

Documents

This scope was carved out of HT942526SCIRPTRA.

The full solicitation package (2 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

DoW Spinal Cord Injury, Translational Research Award

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Organization & Contact Information

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AgencyDepartment Of Defense → Department Of The Army -- Usamraa
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → Department Of The Army -- Usamraa
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Office AddressN/A
ContactsNo contact information available

Full Description

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Performs recruitment and retention of study participants for prime contractors on FY26 Spinal Cord Injury Research Program (SCIRP) projects. Manages administration of pilot clinical trials, including screening based on inclusion/exclusion criteria and coordination of visits. Utilizes patient recruitment databases and decentralized clinical trial (DCT) tools. Requires IRB approval and GCP certification. Delivers recruited study population and retention reports.

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