TBICoE Clinical Research Coordinator - Onsite

Odyssey; Fort Bragg (NC); On-site; USD 55,000 - 85,000; Full time

Job summary

Odyssey is seeking a Clinical Research Coordinator to coordinate TBICoE clinical investigations in TBI, brain health, and related outcomes. The role ensures compliance with local, state, and federal regulations and is onsite at Fort Bragg, NC.

You will support investigators, manage regulatory files, recruit participants, obtain informed consent, assist with data collection and analysis, and help with grant proposals and study documentation.

Qualifications

• 3–5 years of clinical investigations experience required.
• Prior experience within DoD/VA systems preferred.

Responsibilities

• Coordinate TBICoE clinical investigations and ensure regulatory compliance.
• Assist investigators with protocol submissions and IRB processes.
• Maintain regulatory files and participant recruitment, informed consent.
• Support data collection, analysis, and reporting of study results.
• Assist with grant proposals and project documentation.

Skills

Communication

Analytical skills

Team collaboration

Attention to detail

Microsoft Office

Education

Bachelor’s degree in biology/psychology or related health/science

Master’s degree preferred

Human Subjects training completed

Tools

Microsoft Office

Clinical trial management systems (CTMS)

Job description

Odyssey is seeking a Clinical Research Coordinator to coordinate TBICoE clinical investigations in TBI, brain health, and related outcomes. The role ensures compliance with local, state, and federal regulations and is onsite at Fort Bragg, NC.

You will support investigators, manage regulatory files, recruit participants, obtain informed consent, assist with data collection and analysis, and help with grant proposals and study documentation.