Senior Clinical Research Coordinator - DoD
Kelly, Portsmouth, VA, United States
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.
This is 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
Senior Clinical Research Coordinator.
This is an on-site position in Portsmouth, VA.
This is 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