Research Lab Technician I

The Geneva Foundation•San Antonio, TX

10d•$17 - $21

About The Position

The Research Laboratory Technician I will provide technical knowledge and expertise in clinical laboratory analysis by assisting with bench top experiments, preparing and assisting with the experiments, collecting and analyzing data, and preparing reports. About the Project AREVA (Autonomous Reanimation and Evacuation Research Institute and Innovation Center) is a program of The Geneva Foundation. AREVA advances innovative solutions in wearable medical technologies, polytrauma management, and critical care to address the unique challenges of combat and austere environments. With a focus on pioneering portable extracorporeal life support (ECLS) systems and autonomous critical care technologies, AREVA’s research initiatives ensure rapid, effective responses to critical care challenges, enhancing survivability and operational success in the most demanding environments. Mission: To enable the research-to-practice translation of novel life-saving interventions in critical care through the development of clinically relevant translational trauma models and subsequent clinical trials. Impact: AREVA bridges the gap between innovation and application, transforming critical care for combat-relevant trauma with physician-led research that delivers scalable, life-saving solutions at ground level and high altitudes.

Requirements

Bachelor’s degree or equivalent work experience required
1 year experience in biomedical or research laboratory preferred
Non-profit, research, or healthcare experience desired
Demonstrate competence in oral and written communication
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Strong data management and processing skills
Knowledge of Military Operational Planning, the Military Health System and the Military Medical Logistics System preferred
Experience in performing complex chemical, biological, hematological, immunologic, microscopic, and bacteriological tests desired
Familiarity with medical terminology and abbreviations

Responsibilities

Provide technical knowledge and expertise in clinical laboratory analysis.
Write referenced clinical treatment briefs using Government provided methodologies and formats
Perform preliminary research, information gathering, and information packaging in preparation for the Clinical Panels, as needed
Assist the production team with data input
Provide technical knowledge and expertise in clinical laboratory analysis with expert guided recommendations for required tasks, length of tasks, responsible treaters, essential characteristics and material assignments
Adheres to Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), International Air Transportation Association (IATA) Good Laboratory Practices (GLP) and infection control procedures
Demonstrate proficiency in performing basic study related procedures as required
Execution and maintenance of research study
Manage study documentation to include accurate and timely filing
Collection of data and data entry
Perform bioassays of tissue culture and rodent tissues, when applicable to protocol
Responsible for cleaning, disinfecting and maintenance of all clean rooms and equipment
Assist with receipt and inspection of raw materials, lab ordering and stocking, as requested
Process and ship samples according to all regulations and protocol requirements
Document all correspondence and communication pertinent to the research
Interact and communicate effectively with PI, other site personnel, research participants, The Geneva Foundation and the study sponsor
Comply with all the rules and regulations as applicable to assigned duty station
Assist in the preparation and analysis of laboratory experiments, as requested
Maintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.)