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Clinical Data Management Support Service

Overview


Healthcare Services, Wellness & Biotech
Bethesda, Maryland, United StatesPosted: June 9th, 2026Deadline: June 15th, 2026

Fit Score


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SUMMARY


Seeking a vendor to deliver comprehensive clinical data management support services for a government authority's research program in Maryland.

KEY REQUIREMENTS


CONTRACT DURATION


60 months

TIMELINE


Capability statements are due by June 15th, 2026, at 3:00 PM EDT.

Phase-in services must be completed within 30 calendar days after contract award.

Phase-out plan must be provided no later than 90 calendar days prior to contract expiration.

Issuing Agency


National Institutes Of Health

Organization overview and procurement intelligence available on paid plans.

DESCRIPTION


A government authority in Maryland seeks a vendor to provide comprehensive clinical data management support services for its clinical research program. Responsibilities include managing all data management functions, utilizing both current and legacy databases, and implementing robust quality assurance measures.

The selected partner will gather and enter protocol data into databases based on the requirements of each clinical protocol. Additionally, the vendor will develop and structure protocol-specific data management processes and prepare relevant data and reports for audits conducted by regulatory agencies and sponsors. The scope also involves providing overviews of data management processes to new clinical teams and supporting various data management activities for transplant-related protocols. The term of the contract is for one year.

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Frequently asked questions

When is the submission deadline?
Submissions are due June 15, 2026.
Who issued this RFP?
It was issued by National Institutes Of Health. The work is located in Bethesda, Maryland, United States.
Who is a good fit for this opportunity?
  • Experience in clinical data management within healthcare or research settings
  • Familiarity with both legacy and modern database systems
  • Proven ability to support regulatory audits and quality assurance
  • History of supporting transplant or protocol-driven clinical studies
  • Qualified to work with government health authorities

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