Clinical Research Coordinator

Clearance Level
San Antonio, Texas
Onsite Workplace
Key Skills For Success

Case Report Forms

Clinical Research

Good Clinical Practice (GCP)

REQ#: RQ142863
Public Trust: NACLC (T3)
Requisition Type: Regular
Your Impact

Own your opportunity to work alongside federal civilian agencies. Make an impact by providing services that help the government ensure the well being of U.S. citizens.

Job Description

Clinical Research Coordinator/Scientist Associate

Seize your opportunity to make a personal impact as a Clinical Research Coordinator supporting the 59th Medical Wing in the Science & Technology Office.

GDIT is your place to make meaningful contributions to challenging projects and grow a rewarding career.

The 59th Medical Wing Science and Technology (ST) office advises and conducts clinical and translational research on matters pertaining to the medical aspects of the Air Expeditionary Force and the health of Air Force (AF) personnel and beneficiaries. In order to support the required research, ST offices conduct translational research in the areas of emergency medical care, combat casualty care, force health protection, restorative medicine, clinical and rehabilitative medicine and specialty centers.

The Clinical Research Coordinator will support Government directors,

Principal Investigators (PIs,) in the planning, programming, and execution of

clinical research projects and protocols and associated activities.


  • Maintains study records in accordance with protocols, study schedules, participant observations, and provides follow up documentation to the PI
  • For human research studies, assists with study enrollment and activities related to the conduct of the study
  • Coordinates one (1) to several simultaneous projects for the PI/director; confers with investigator on experimental design; provides instruction on various research laboratory techniques, and study participant contact procedures
  • Organizes research information; manages reporting and data collection.
  • Monitors research study budget
  • Research equipment/supply catalogs and recommend purchase requests for projects/protocols in accordance with the IRB
  • Documents all regulatory research and administrative actions to ensure study compliance
  • Prepares/delivers required reports and other research documentation to PI.
  • Prepares correspondence, builds study files, develop schedules, and presentation graphics to support the research study
  • Uses available software systems, specifically which includes the current accounts tracking systems, publication submissions, purchase orders, credit card purchases, and preparation of forms for incoming and out coming funds
  • May sometimes require evening or weekend hours


  • Education: Bachelor's degree in Biological Sciences or a closely related field, Master's degree preferred
  • Required Experience: 2+ years of clinical research experience
  • Required Technical Skills: Knowledge of CFR, GCP and ICH guidelines; Demonstrated FDA regulatory experience; Computer skills including a least intermediate level experience with Excel and other Microsoft Office Software.
  • Certification or Training: Must have or successfully complete CITI training (within 6 months of hire) and keep current; Completed GCP training and familiar with GCP in practice
  • Security Clearance Level: Ability to obtain/maintain a favorable T3 security investigation
  • Required Skills and Abilities: Demonstrate competence in oral and written communication
  • Location: Lackland Air Force Base/San Antonio, TX
  • US Citizenship Required


  • 401K with company match
  • Comprehensive health and wellness packages
  • Internal mobility team dedicated to helping you own your career
  • Professional growth opportunities including paid education and certifications
  • Cutting-edge technology you can learn from
  • Rest and recharge with paid vacation and holidays






Work Requirements
Years of Experience

2 + years of related experience

* may vary based on technical training, certification(s), or degree

Travel Required



U.S. Citizenship Required

About Our Work

We are GDIT. The people supporting some of the most complex government, defense, and intelligence projects across the country. We deliver. Bringing the expertise needed to understand and advance critical missions. We transform. Shifting the ways clients invest in, integrate, and innovate technology solutions. We ensure today is safe and tomorrow is smarter. We are there. On the ground, beside our clients, in the lab, and everywhere in between. Offering the technology transformations, strategy, and mission services needed to get the job done.

COVID-19 Vaccination

GDIT does not have a vaccination mandate applicable to all employees. To protect the health and safety of its employees and to comply with customer requirements, however, GDIT may require employees in certain positions to be fully vaccinated against COVID-19. Vaccination requirements will depend on the status of the federal contractor mandate and customer site requirements.

GDIT is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status, or any other protected class.