Clinical Research Coordinator

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

Position Summary

Odyssey is looking for a Clinical Research Coordinator to coordinate and assure the integrity of all activities associated with conducting Trauma Brain Injury Center of Excellence (TBICoE) clinical investigations in TBI, brain health, and related outcomes. The candidate will ensure compliance with local, state, and/or federal regulatory requirements. This job is onsite at Ft Bragg, NC.

Responsibilities

• Coordinates and assures integrity of all activities associated with conducting TBICoE TBI clinical investigations as it relates to compliance with local, state, and/or federal regulatory requirements.
• Assists Principal / Associate Investigators in the preparation and submission of clinical protocols, consent forms and other documents to the scientific review committee, IRB and other regulatory organizations.
• Prepares requests for actions/proposals to include assisting with and providing coordination for grant proposal applications and their associated documentation and requirements as facilitates the flow and approval processes for relevant projects as needed or requested.
• Maintains regulatory files related to TBICoE clinical investigations.
• Communicates with research participants, staff, regulatory affairs and data management groups, laboratory and clinical investigators, management and outside collaborators.
• Recruits, interviews, and screens TBICoE clinical research study volunteers, administers and obtains informed consent.
• Assists in the collection and analysis of data to evaluate volunteer eligibility for enrollment.
• Assists with TBI Program/Quality Improvement initiatives or implementation science studies.
• Assists in the collection, analysis and interpretation of laboratory and clinical data obtained during a medical evaluation, reporting significant values, findings and events that require prompt attention to clinical investigators.
• Assists with the documentation and reporting of adverse events, completes and reviews subject eligibility criteria, protocol compliance, omissions, and errors, and submits these forms as needed.
• Prepares and maintains written and electronic volunteer databases/logs.
• Performs data extraction and chart reviews of patients’ and/or research participant’s medical records or other relevant record/systems, as applicable.
• Ensures that research records are stored and secured properly and that inventory and records are updated and properly maintained.
• Conducts data verification as indicated, documents, assists the investigator and protocol coordinator with questions, may transcribe and resolve queries of data on study forms (hardcopy and/or electronic).
• Prepares documents, under direction of project leads; trains incoming staff on study procedures and SOPs.
• Assists with statistical analyses and descriptive data capture under direction of project leads. Works with the site senior clinical research director and other senior research leads for the collection, documentation and analysis of metrics to ensure a successful research program.
• Contingent upon contract award.

Qualifications

• Citizenship: Must be a US citizen.
• Clearance: Ability to obtain Secret.
• Education: Bachelor’s Degree or higher in biology, psychology or related health/social science required. Master’s degree preferred. Must have Human Subjects training completed.
• Years of Experience: 3-5 years clinical investigations experience required. Prior experience within the DoD/VA systems of care preferred.
• Certifications: Certification as a Clinical Research Coordinator (CCRC), Clinical Research Professional (CCRP) and/or Clinical Research Associate (CCRA) preferred (must maintain continuing education credit sufficient to maintain certification when applicable).

Other Requirements

• Excellent communication skills, basic clinical acumen, knowledge of universal precautions, organizational skills and proficiency in research conduct are required.
• Knowledge of standard qualitative and quantitative data collection techniques; ability to follow general instructions; works effectively in a team and independently; demonstrates strong communication, writing and analytical skills. Familiarity with social science research methodology is required. Ability to follow detailed instructions.
• Must be able to work comfortably with computer software, including Microsoft Office and familiarity with basic statistical analyses.
• Adhere to legal, professional and ethical codes with respect to confidentiality and privacy.
• Physical capabilities: Must be able to sit and stand for long periods of time. Must be able to carry light items – up to 25 lbs.
• Work environment: Office clinical and hospital environment. May encounter patients who are confused, agitated or abusive.
• Must be available to travel locally, regionally and nationally. May include hours in the late afternoons, evenings, and/or weekends, depending on study assessments and participant scheduling requirements.

Additional Information

Location: Naval Medical Center San Diego, 34800 Bob Wilson Drive, San Diego, CA.

Travel: NA

Remote, Onsite, or Hybrid: Onsite

Contingent upon contract award.

Company Overview

Odyssey is a world‑class technical, engineering, and integration company serving the warfighting ecosystem with airborne integration, ISR, C2, and warfighter readiness capabilities. Odyssey meets the military’s operational needs by integrating layered defense systems from equipment, technology, and services to data, information, and business operations. We streamline defense acquisition and sustainment, engineering the technical battlefield with domain‑specific proficiency to ensure lethality. Odyssey is dedicated to excellent contract execution, peak organizational performance, and fostering a workplace built on employee care.

Odyssey is proud to live out our core values of commitment, ambition, and respect in our work and communities through OdysseyCares, a philanthropic group focused on giving back through direct donations, an employer match program, and volunteering events.

Please note: Final compensation for this position will be determined by various factors such as the Federal Government contract labor categories and contract wage rates, relevant work experience, specific skills and competencies, geographic location, education, and certifications.