Senior Clinical Research Coordinator – DoD

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Kelly Government Solutions is a strategic supplier and business partner to the federal government and its key suppliers. Our DoD client is seeking a Senior Clinical Research Coordinator. This is an on-site position in Portsmouth, VA.

POSITION OFFERS

  • Competitive compensation and comprehensive benefit package
  • Relocation Assistance
  • Optional health, vision, and dental plans
  • Paid leave, paid federal holidays, and 401K plan.

PRIMARY RESPONSIBILITIES

  • Provide research, regulatory, and administrative support for IRB and IACUC-approved protocols, ensuring compliance with federal and local guidelines.
  • Serve as a liaison between research teams, PIs, and regulatory authorities.
  • Coordinate study enrollment, subject screening, data collection, participant follow-up, and investigational product accountability per protocol requirements.
  • Maintain accurate study records, prepare regulatory reports, and support audits, inspections, and research training initiatives.
  • Utilize standard office and clinical information systems (e.g., Word, Excel, CHCS-I, AHLTA) to manage study data and documentation.
  • Collaborate with PIs and research staff on study development, funding applications, participant education, and protocol close-out activities, while ensuring HIPAA compliance and patient confidentiality.
  • Ensure clinical trial participant safety and data integrity through site visits, source data verification (SDV), and protocol compliance

REQUIREMENTS

  • Minimum 5-10 years of experience as Clinical Research Coordinator
  • Active Public Trust or Secret Clearance
  • Minimum of 2 years of clinical site monitoring experience in a clinical research environment

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Company: Kelly
Apply for the Senior Clinical Research Coordinator – DoD
Location: Cornholme
Job Description:

Kelly Government Solutions is a strategic supplier and business partner to the federal government and its key suppliers. Our DoD client is seeking a Senior Clinical Research Coordinator. This is an on-site position in Portsmouth, VA.

POSITION OFFERS

  • Competitive compensation and comprehensive benefit package
  • Relocation Assistance
  • Optional health, vision, and dental plans
  • Paid leave, paid federal holidays, and 401K plan.

PRIMARY RESPONSIBILITIES

  • Provide research, regulatory, and administrative support for IRB and IACUC-approved protocols, ensuring compliance with federal and local guidelines.
  • Serve as a liaison between research teams, PIs, and regulatory authorities.
  • Coordinate study enrollment, subject screening, data collection, participant follow-up, and investigational product accountability per protocol requirements.
  • Maintain accurate study records, prepare regulatory reports, and support audits, inspections, and research training initiatives.
  • Utilize standard office and clinical information systems (e.g., Word, Excel, CHCS-I, AHLTA) to manage study data and documentation.
  • Collaborate with PIs and research staff on study development, funding applications, participant education, and protocol close-out activities, while ensuring HIPAA compliance and patient confidentiality.
  • Ensure clinical trial participant safety and data integrity through site visits, source data verification (SDV), and protocol compliance

REQUIREMENTS

  • Minimum 5-10 years of experience as Clinical Research Coordinator
  • Active Public Trust or Secret Clearance
  • Minimum of 2 years of clinical site monitoring experience in a clinical research environment

#J-18808-Ljbffr…

Posted: May 2nd, 2026