The Geneva Foundation · 2 months ago
Research Lab Technician I
The Geneva Foundation is focused on advancing innovative solutions in critical care and wearable medical technologies. The Research Laboratory Technician I will provide technical expertise in clinical laboratory analysis, assist with experiments, collect and analyze data, and prepare reports to support research initiatives in critical care environments.
Clinical TrialsEducationNon Profit
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.)
Qualification
Required
Bachelor's degree or equivalent work experience required
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
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.)
Preferred
1 year experience in biomedical or research laboratory preferred
Non-profit, research, or healthcare experience desired
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
Company
The Geneva Foundation
The Geneva Foundation is a non-profit organization that supports medical research and in the U.S. military.
H1B Sponsorship
The Geneva Foundation has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (1)
2024 (6)
2023 (2)
2022 (1)
2021 (1)
2020 (1)
Funding
Current Stage
Growth StageLeadership Team
Recent News
Birmingham Business Journal
2025-01-20
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