Administrative Clinical Research Coordinator

CHENEGA RELIABLE SERVICES, LLC JBSA Lackland, AFB The Clinical Research Coordinator, Administrative shall support Government directors, PIs, in the planning, programming, and execution of clinical research projects and protocols and associated activities. Responsibilities Maintains study records in accordance with protocols, study schedules, participant observations, and provides follow up documentation to the PI. Assists with study enrollment and activities related to the conduct of the study, for human research studies. 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. Researches 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 require occasional weekend and evening hours. Other duties as assigned Qualifications High School Diploma Minimum of two (2) years experience in clinical research. Complete Collaborative Institutional Training Initiative (CITI) training and remain current, Preferred. Knowledge, Skills and Abilities Demonstrate competence in oral and written communication Possess organization, attentive to detail, and possess a positive, friendly and professional demeanor. Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software Knowledge of Code of federal Regulation (CFR), Good Clinical Practice (GCP) and International Council for Harmonization (ICH) guidelines. Demonstrated FDA regulatory experience. Physical Demands (The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) While performing the duties of this Job, the employee is regularly required to sit and talk or hear. The employee may use repeated motions that include the arms, wrists, hands and/or fingers. The employee is occasionally required to walk, stand, climb, balance, stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision. Any estimated salary provided by this job board may not align with Chenega's compensation program. Please apply to connect with a recruiter who can provide more details.

Created: 2026-03-05