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Clinical Research & Patient Outcome Studies

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Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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This subcontract, titled Clinical Research and Patient Outcome Studies, supports the Department of the Army USAMRAA in conducting research focused on melanoma projects. The scope of work involves studying the preservation of function, quality of life, and symptom management, with a specific emphasis on managing patient recruitment, longitudinal studies, and psychological impact assessments through standardized survey instruments. The contractor is responsible for delivering clinical study reports and patient outcome data while adhering to strict regulatory requirements, including IRB approval, HIPAA compliance, and Good Clinical Practice standards. The project is categorized under NAICS code 621391 and was posted on May 5, 2026.

General Info

Subcontract for USAMRAA melanoma research focusing on patient outcomes, recruitment, and clinical reporting.

Agency

Department Of Defense → Department Of The Army -- Usamraa

NAICS

621391 - Offices of Podiatrists

Place of Performance

Not specified

Set-Aside

NONE

Documents

This scope was carved out of HT942526MRPIA.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

DoW Melanoma Research Program Idea Award

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Timeline

PostedMay 5

subcontract

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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 / AgencyDepartment Of Defense → Department Of The Army -- Usamraa

Office AddressN/A

ContactsNo contact information available

Full Description

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Performs research on preservation of function, quality of life, and symptom management for prime contractors on Army Medical Research melanoma projects. Manages patient recruitment, longitudinal studies, and psychological impact assessments using standardized survey instruments. Requires IRB approval, HIPAA compliance, and GCP standards. Delivers clinical study reports and patient outcome data.

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