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Clinical Research Organization (CRO) Services

Active

Grant

Response Deadline10/01/2026, 04:00:00 AM UTC

Contract Overview

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

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This subcontract for Clinical Research Organization (CRO) Services supports the Department of Defense and the Department of the Army USAMRAA. The selected provider will perform end-to-end management and execution of clinical trials for prime contractors on OCRP projects, with a primary focus on patient recruitment, site monitoring, and clinical data analysis. The contractor is responsible for delivering completed clinical trial data and statistical analysis reports while ensuring strict adherence to GCP, GLP, and GMP guidelines. This opportunity falls under NAICS code 541711 and has a response deadline of October 1, 2026.

General Info

CRO services for DoD/USAMRAA clinical trials focusing on recruitment, monitoring, and data analysis.

Agency

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

NAICS

541711 - Research and Development in BiotechnologyView NAICS

Place of Performance

Not specified

Set-Aside

NONE

Documents

This scope was carved out of HT942526OCRPCTA.

The full solicitation package (3 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

DoW Ovarian Cancer, Clinical Trial Award

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Timeline

PostedMay 4

subcontract

Response DeadlineOct 1

Submission deadline

Response Deadline

10/01/2026, 04:00:00 AM UTCin 21 days

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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 end-to-end management and execution of clinical trials for prime contractors on Department of Defense OCRP projects. Manages patient recruitment, site monitoring, and clinical data analysis. Ensures compliance with Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Manufacturing Practice (GMP) guidelines. Delivers completed clinical trial data and statistical analysis reports.

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