Clinical Research Coordinator

Type of Requisition:

Regular

Clearance Level Must Currently Possess:

None

Clearance Level Must Be Able to Obtain:

None

Suitability:

Public Trust/Other Required:

NACLC (T3)

Job Family:

Scientists

Job Qualifications:

Skills:

Case Report Forms, Clinical Research, Good Clinical Practice (GCP), Researching

Certifications:

Experience:

2 + years of related experience

US Citizenship Required:

Yes

Job Description:

GDIT's Military Health team is hiring a Senior Clinical Research Administration Manager to support research within the Air Force- 59th Medical Wing located, on-site, at Joint Base San Antonio- Fort Sam Houston, TX.

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.

HOW A CLINICAL RESEARCH COORDINATOR WILL MAKE AN IMPACT:

• 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

WHAT YOU’LL NEED TO SUCCEED:

• Bachelor's degree in Biological Sciences or a closely related field, Master's degree preferred

• 2+ years of clinical research experience

• 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.

• Must have or successfully complete CITI training (within 6 months of hire) and keep current

• Completed GCP training and familiar with GCP in practice

• US citizenship with the ability to obtain/maintain a favorable T3 security investigation

GDIT IS YOUR PLACE:

• 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

#MilitaryHealthGDITJobs

#59thMDWGDITJOBS

#GDITFedHealthJobs  

#GDITHealth

The likely salary range for this position is $45,698 - $53,763. This is not, however, a guarantee of compensation or salary. Rather, salary will be set based on experience, geographic location and possibly contractual requirements and could fall outside of this rang