Clinical Research Coordinator: TBICoE (Onsite)

General Dynamics Information Technology; Fort Bragg (NC); On-site; USD 58,000 - 78,000; Full time

Job summary

General Dynamics Information Technology (GDIT) is seeking a Clinical Research Coordinator to join the TBICoE team at Fort Bragg, NC. The CRC will coordinate TBICoE clinical investigations, ensure regulatory compliance, and manage consent processes for trauma-related brain injury studies.

The role requires a bachelor's degree in a related field, Human Subjects training, and 3+ years of clinical investigations experience. Onsite work with potential NACLC (T3) eligibility is involved.

Qualifications

• Bachelor's degree or higher in biology, psychology or related science.
• Human Subjects training completed.
• 3+ years clinical investigations experience.
• 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 MS Office (Word, Excel, Outlook, PowerPoint).

Responsibilities

• Coordinates and assures integrity of TBICoE TBIC research activities with local, state, and federal regulatory requirements.
• Assists investigators with preparation and submission of protocols, consent forms and related documents to IRB and committees.
• Facilitates grant proposals and related documentation as needed.
• Maintains regulatory files for TBICoE clinical investigations.
• Communicates with participants, staff, regulatory affairs, data management, and investigators.
• Recruits, interviews, screens volunteers, and administers informed consent.
• Assists in data collection and analysis to evaluate eligibility and outcomes.
• Supports TBICoE program/Quality Improvement initiatives at the site.
• Collects, analyzes and interprets laboratory and clinical data.
• Documents adverse events and ensures protocol compliance and data integrity.
• Prepares and maintains volunteer databases/logs; performs data extraction and chart reviews.
• Trains incoming staff on study procedures and SOPs.
• Supports statistical analyses and data capture under direction of project leads.
• Adheres to confidentiality and privacy requirements; ensures security of records.

Skills

Clinical Research

Informed Consent

IRB (Inactive)

Participant Recruiting

Education

Bachelor's degree or higher in biology, psychology or related science

Job description

General Dynamics Information Technology (GDIT) is seeking a Clinical Research Coordinator to join the TBICoE team at Fort Bragg, NC. The CRC will coordinate TBICoE clinical investigations, ensure regulatory compliance, and manage consent processes for trauma-related brain injury studies.

The role requires a bachelor's degree in a related field, Human Subjects training, and 3+ years of clinical investigations experience. Onsite work with potential NACLC (T3) eligibility is involved.