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Clinical Trial Site Management and Coordination

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Contract Overview

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This subcontract for Clinical Trial Site Management and Coordination supports the National Institutes of Health and the National Institute on Alcohol Abuse and Alcoholism. The selected provider will handle the operational execution of clinical trials focused on alcohol misuse and Alcohol Use Disorder, working under prime contractors to recruit and screen participants, administer trial protocols, and collect data. All activities must adhere to NIH Research Methods Resources, requiring strict compliance with IRB approval and GCP certification to ensure participant safety and data integrity. The scope of work includes the use of secure medical record storage and clinical data capture systems to manage information, culminating in the delivery of completed clinical trial datasets and comprehensive safety reports. This opportunity falls under NAICS code 541715 and is associated with the Department of Health and Human Services. Interested parties should note the response deadline of January 27, 2027.

General Info

Subcontract for NIH clinical trial site management regarding alcohol misuse, due January 27, 2027.

Agency

Department Of Health And Human Services → National Institutes Of Health

Place of Performance

Not specified

Set-Aside

NONE

Documents

This scope was carved out of RFA-AA-28-001.

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

View the prime solicitation

Specialized Alcohol Research Centers (P50 Clinical trial Optional)

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Timeline

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → National Institutes Of Health
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Health And Human Services → National Institutes Of Health
Office AddressN/A
ContactsNo contact information available

Full Description

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Performs operational execution of NIH-defined clinical trials for prime contractors on NIH/NIAAA alcohol misuse and Alcohol Use Disorder (AUD) projects. Recruits and screens participants, administers trial protocols, collects data, and monitors participant safety per NIH Research Methods Resources. Utilizes clinical data capture systems and secure medical record storage. Requires IRB approval and GCP certification. Delivers completed clinical trial datasets and safety reports.

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