Research Assistant

Position Summary

Responsibilities

• Performs data entry for clinical investigation research projects and maintains databases meticulously including recruitment/screening of potential study subjects; data maintenance; scheduling and testing spreadsheets for participant consenting, study evaluations, and follow up study visits.
• Performs data entry quality checks and quality assurance.
• Affords assistance in the preparation of technical reports, summaries, and protocols.
• Maintains study related documents and supplies; secures, organizes and documents IAW all federal/state/installation regulations.
• Creates, collects, disseminates, maintains appropriate files of study data and assists with review and completion of study manuals and SOPs.
• Screens, consents, and/or schedules potential research participants for testing or evaluation.
• Facilitates follow-up assessment reminders, scheduling, and testing with all related documentation.
• Extracts data from patient and/or research participant medical records; transcribes and resolves data queries in study forms (hardcopy and/or electronic); prepares documents, under direction of project leaders; prepares data for statistical analyses and reports descriptive data to be used in research/clinical investigations/studies reports.
• Maintains awareness of and compliance with human subjects’ research regulatory issues.
• Communicates regularly with study team, under direction of project leaders, in writing and verbally as needed.
• May assist with TBI program/project improvement initiatives at the site.
• Affords assistance with literature searches, obtaining articles for review.
• Affords assistance with obtaining and collating materials for reports, manuscripts and for meetings.

Qualifications

• Citizenship: Must be a US citizen.
• Clearance: Ability to Obtain Secret.
• Education: Bachelor’s Degree required.
• Human Subjects training required.
• Current certification in Basic Life Support if working in a hospital environment.
• Years of Experience: 6 months to 2 years of experience in research/clinical investigations/studies required.
• Prior experience within the DoD/VA systems of care preferred.
• Certifications: Must complete CITI/ HIPAA training.

Additional Information

• Location: 2843 Normandy Drive, Ft. Bragg, NC
• Travel: Some required.
• Remote, Onsite, or Hybrid: Onsite

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.