ABSS Solutions, Inc. (ASI), is seeking a full-time Clinical Research Coordinator to join our team in providing Medical Research support to the 59th Medical Wing in San Antonio, Texas. ASI administers a comprehensive research and development contract providing an array of research projects for customers across the DoD space. Our research teams work with educational institutions and other third party organizations to maximize readiness, and resilience for the men and women of our armed forces..

Job Roles and Responsibilities:

• Supports Government directors, 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 require occasional weekend and evening hours.

Minimum Qualification and Experience:
• Required: B.S in Biological Sciences or a closely related field; Masters highly preferred.
• 2-4 years’ minimum experience in clinical research.
• Demonstrate competence in oral and written communication.
• Must be organized, 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 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