Clinical Research Coordinator (CRC)

GDIT's Military Health Team is hiring a Clinical Research Coordinator (CRC) to join their current research team to help carry out Traumatic Brain Injury Research for the Traumatic Brain Injury Center of Excellence (TBICoE) located at Ft. Bragg in Fayetteville, North Carolina.

The CRC is responsible for coordinating and assuring integrity of all activities associated with conducting TBICoE clinical investigations in the area of TBI. They will ensure compliance with local, state, and/or federal regulatory requirements.

Key responsibilities:

• Coordinate and assure integrity of all activities associated with conducting TBICoE TBI clinical investigations
• Assist Principal / Associate Investigators in the preparation and submission of clinical protocols, consent forms and other documents
• Prepare requests for actions/proposals and provide coordination for grant proposal applications
• Maintain regulatory files related to TBICoE clinical investigations
• Communicate with research participants, staff, regulatory affairs and data management groups
• Recruit, interview, and screen TBICoE clinical research study volunteers
• Assist in the collection and analysis of data to evaluate volunteer eligibility for enrollment
• May assist with TBI Program/Quality Improvement initiatives
• Assist in the collection, analysis and interpretation of laboratory and clinical data
• Assist with the documentation and reporting of adverse events
• Prepare and maintain written and electronic volunteer databases/logs
• Perform data extraction and chart reviews of patients' and/or research participant's medical records
• Ensure that research records are stored and secured properly
• Conduct data verification and assist the investigator and protocol coordinator with questions
• Prepare documents and train incoming staff on study procedures and SOPs
• Assist with statistical analyses and descriptive data capture

Requirements:

• Bachelor's degree or higher in biology, psychology or related science
• 3+ years clinical investigations experience
• Human Subjects training completed
• Knowledge of standard qualitative and quantitative data collection techniques
• Good writing and analytical skills
• Familiarity with social science research methodology
• Ability to work comfortably with computer software, including Microsoft Word, Excel, Outlook and PowerPoint

Preferred qualifications:

• Master's degree
• Certification as a Clinical Research Coordinator (CCRC), Clinical Research Professional (CCRP) and/or Clinical Research Associate (CCRA)
• Prior experience within the DoW/VA systems of care

The likely salary range for this position is $57,824 - $78,200.