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Biostatistical Analysis for Prostate Cancer Clinical Trials

Active
Federal

Contract Overview

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

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The contract seeks expert biostatistical support for prostate cancer clinical trials, encompassing full lifecycle contributions such as trial design, survival analysis, and statistical reporting across multi-site studies. The work involves providing specialized analytical expertise to ensure methodological rigor and regulatory compliance in generating reliable clinical outcomes data. This subcontract is issued under the Department of Veterans Affairs through the 245-NETWORK Contract Office 5 and falls under NAICS code 541714, which designates research and development in the physical, engineering, and life sciences. The solicitation was posted on June 26, 2026, with a deadline for responses on July 12, 2026, at 12:00 PM. The place of performance and contact details are not specified, indicating flexibility in execution location, while the nature of the work remains focused on delivering high-quality statistical services tailored to veteran-focused oncology research.

General Info

Expert biostatistical support for VA prostate cancer trials including design, analysis, and regulatory compliance.

Agency

Department Of Veterans Affairs → 245-NETWORK Contract Office 5 (36C245)View Agency

NAICS

541714 - Research and Development in Biotechnology (except Nanobiotechnology)View NAICS

Place of Performance

MD

Set-Aside

NONE

Documents

(0)

No documents available

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Timeline

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Organization & Contact Information

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AgencyDepartment Of Veterans Affairs → 245-NETWORK Contract Office 5 (36C245)
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Veterans Affairs → 245-NETWORK Contract Office 5 (36C245)
View Agency Profile
Office AddressN/A
ContactsNo contact information available

Full Description

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Provide expert biostatistical analysis and consulting for prostate cancer clinical trials, including trial design, survival analysis, and statistical reporting across multi-site studies.

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