Onsite Clinical Research Coordinator, TBICoE (TBI)

General Dynamics Information Technology

North Carolina

On-site

USD 58,000 - 78,000

Full time

6 days ago
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Job summary

General Dynamics Information Technology is seeking a Clinical Research Coordinator to support Traumatic Brain Injury research at Fort Bragg, NC. The CRC will coordinate TBICoE clinical investigations, ensure regulatory compliance and assist investigators with protocols and consent forms.

Responsibilities include participant recruitment, data collection, adverse event reporting and training of new staff. Requires 3+ years in clinical investigations and Human Subjects training, with US citizenship

Qualifications

  • Bachelor’s degree or higher in biology, psychology or related science.
  • Must have 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 computer software, including Microsoft Word, Excel, Outlook and PowerPoint.

Responsibilities

  • Coordinates and assures integrity of TBICoE TBI clinical investigations with regulatory compliance.
  • Assists investigators in preparing protocols, consent forms and documents for IRB and regulatory bodies.
  • Supports grant proposal prep and coordination; facilitates project approval processes.
  • Maintains regulatory files related to TBICoE investigations.
  • Communicates with participants, staff, regulatory, data management and clinical teams.
  • Recruits, interviews and screens TBICoE volunteers; administers and obtains informed consent.
  • Assists with data collection and analysis to evaluate volunteer eligibility for enrollment.
  • Supports TBI Program/Quality Improvement initiatives at the site.
  • Collects, analyzes and interprets lab and clinical data; reports significant values to investigators.
  • Documents and reports adverse events; ensures eligibility criteria and protocol compliance; updates forms as needed.
  • Prepares and maintains volunteer databases/logs; performs data extraction and chart reviews.
  • Ensures research records are stored securely; maintains inventory and records.
  • Trains incoming staff on study procedures and SOPs; assists with statistical analyses and data capture.
  • Adheres to confidentiality, privacy and ethical standards; US citizenship to pass a T3 security investigation.

Skills

Clinical Research
Informed Consent
IRB (Inactive)
Participant Recruiting

Education

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

Tools

Microsoft Word
Excel
Outlook
PowerPoint

Job description

General Dynamics Information Technology is seeking a Clinical Research Coordinator to support Traumatic Brain Injury research at Fort Bragg, NC. The CRC will coordinate TBICoE clinical investigations, ensure regulatory compliance and assist investigators with protocols and consent forms.

Responsibilities include participant recruitment, data collection, adverse event reporting and training of new staff. Requires 3+ years in clinical investigations and Human Subjects training, with US citizenship

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