{"id":1161034,"url":"https://alion.io/job/odysseyconsult-clinical-research-coordinator-2","title":"Clinical Research Coordinator","company":{"id":2670648,"name":"Odysseyconsult","domain":"odysseyconsult.com","url":"https://alion.io/company/odysseyconsult","size_band":"1001-5000","is_staffing_agency":false,"is_intermediary":false,"ats_vendor":"iCIMS","truth_index":null},"role":"Administrative","role_family":"Administrative","seniority":"middle","employment_type":null,"work_mode":"on_site","remote_scope":null,"hiring_geo_confidence":"structured","locations":[],"countries":[],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-09-23T23:45:38Z","employer_posted_date":"2026-09-23","last_verified_at":"2026-09-24T02:45:55Z","board_verified":true,"closed_at":null,"days_open":0,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":0},"description":"Position Summary\nOdyssey is looking for a Clinical Research Coordinator to coordinate and assure the integrity of all activities associated with conducting Traumatic 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.\n***Contingent upon contract award***\nResponsibilities\nDuties include, but are not limited to:\nCoordinates 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.\nAssists 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.\nPrepares requests for actions/proposals to include assisting with and providing coordination for grant proposal applications and their associated documentations and requirements as Facilitates the flow and approval processes for relevant projects as needed or requested.\nMaintains regulatory files related to TBICoE clinical investigations.\nCommunicates with research participants, staff, regulatory affairs and data management groups, laboratory and clinical investigators, management and outside collaborators.\nRecruits, interviews, and screens TBICoE clinical research study volunteers, administers and obtains informed consent\nAssists in the collection and analysis of data to evaluate volunteer eligibility for enrollment.\nAssists with TBI Program/Quality Improvement initiatives or implementation science studies.\nAssists in the collection, analysis and interpretation of laboratory and clinical data obtained during a medical evaluation, report significant values, findings and events that require prompt attention to clinical investigators.\nAssists with the documentation and reporting of adverse events, completes and reviews subject eligibility criteria, protocol compliance, omissions, and errors and submits these forms as \nPrepares and maintains written and electronic volunteer databases/logs.\nPerforms data extraction and chart reviews of patients’ and/or research participant’s medical records or other relevant record/systems, as applicable.\nEnsures that research records are stored and secured properly and that inventory and records are updated and properly maintained.\nConducts 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).\nPrepares documents, under direction of project leads. Trains incoming staff on study procedures and SOPs.\nAssists 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.\n***Contingent upon contract award***\nQualifications\nMinimum Required Qualifications\nCitizenship: Must be a US citizen.\nClearance: Ability to Obtain Secret.\nEducation: Bachelor's Degree or higher in biology, psychology or related health/social science required. Master’s degree preferred. Must have Human Subjects training completed.\nYears of Experience: 3-5 years clinical investigations experience required. Prior experience within the DoD/VA systems of care preferred.\nCertifications: 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).\nOther requirements:\nExcellent communication skills, basic clinical acumen, knowledge of universal precautions, organizational skills and proficiency in research conduct are required.\nKnowledge 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.\nMust be able to work comfortably with computer software, including Microsoft Office and familiarity with basic statistical analyses.\nAdhere to legal, professional and ethical codes with respect to confidentiality and privacy.\nPhysical Capabilities: Must be able to sit and stand for long periods of time. Must be able to carry light items - up to 25 lbs.\nWork Environment: Office clinical and hospital environment. May encounter patients who are confused, agitated or abusive. \nMust 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.\nAdditional Information\nLocation: Naval Medical Center San Diego, 34800 Bob Wilson Drive, San Diego, CA.\nTravel: NA\nRemote, Onsite, or Hybrid: Onsite\n***Contingent upon contract award***\nCompany Overview\nOdyssey 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.\nOdyssey 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.\nPlease 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.\n Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities","description_format":"text","description_chars":6487,"description_truncated":false,"requirements":{"experience_years_min":3,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":true},"security_clearance":true,"languages":[]},"benefits":[],"hiring_locations":[{"name":"United States","iso":"US","kind":"country"}],"hiring_excludes":[],"relocation_offered":false,"industries":["Clinical Research","Military","Professional Services","Science & Engineering"],"lifecycle":[{"event":"open","at":"2026-09-23T23:45:38Z"}],"liveness":{"score":86,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.86,"p_room":1,"age_days":0,"expected_fill_days":27,"reasons":["conf:2","win:early","comp:brand"],"computed_at":"2026-09-24T05:24:31Z"},"pay":null,"html_url":"https://alion.io/job/odysseyconsult-clinical-research-coordinator-2","json_url":"https://alion.io/job/odysseyconsult-clinical-research-coordinator-2.json","meta":{"generated_at":"2026-09-24T05:24:31Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers"}}