GDIT is seeking a Clinical Research Coordinator in support of human subject clinical research studies for the 59th Medical Wing (59 MDW) located at Lackland Air Force Base in San Antonio, Texas.
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.
What Youll Be Doing:
Supports the Force Health Protection/Human Performance research portfolio, supporting the Program Manager with tracking and managing financial aspects of clinical research.
Update and maintain quarterly project reports.
Create and distribute funding requests, decision packets, study documents, forecasts, etc.
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 hour
What Youll Need (required):
Bachelors degree in Biological Sciences or a closely related field.
2+ years’ minimum experience in clinical research.
Demonstrate competence in oral and written communication.
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software.
Knowledge of CFR, GCP and ICH guidelines.
Must successfully complete CITI training and remain current.
Completed GCP training and familiar with GCP in practice.
Demonstrated FDA regulatory experience.
What Would Be Even Better (preferred):
Masters degree highly preferred.
Attributes for Success:
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor.
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.
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.