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Clinical Trial Management & Coordination

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This subcontract for Clinical Trial Management and Coordination supports Department of Defense breast cancer research projects under the Department of the Army. The selected provider will perform operational management for prime contractors, which includes coordinating investigators, managing study participants, and ensuring strict adherence to clinical trial protocols. Key responsibilities involve utilizing medical record management software and patient monitoring systems while maintaining full compliance with Good Clinical Practice and Institutional Review Board standards. The contract emphasizes the implementation of women and minority inclusion strategies to ensure diverse participant representation. Deliverables include comprehensive clinical trial data and detailed enrollment reports. This opportunity is categorized under NAICS code 541710, with a response deadline set for September 30, 2026.

General Info

DoD breast cancer research subcontract for clinical trial management and coordination until September 2026.

Agency

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

NAICS

541710 - Research and Development in the Physical, Engineering, and Life SciencesView NAICS

Place of Performance

Not specified

Set-Aside

NONE

Documents

This scope was carved out of HT942526BCRPBTA3.

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

View the prime solicitation

DoW Breast Cancer, Breakthrough Award Level 3

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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 operational management of clinical trials for prime contractors on Department of Defense breast cancer research projects. Coordinates investigators, manages study participants, and ensures adherence to clinical trial protocols. Utilizes patient monitoring systems and medical record management software. Requires GCP and IRB compliance and adherence to women and minority inclusion strategies. Delivers completed clinical trial data and enrollment reports.

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