Kenya Medical Research Institute (KEMRI) is a State Corporation established through the Science and Technology (Amendment) Act of 1979, which has since been amended to Science, Technology and Innovation Act 2013. The 1979 Act established KEMRI as a National body responsible for carrying out health research in Kenya.
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Receive, label, process, and store biological specimens in accordance with study protocols and Good Clinical Laboratory Practice (GCLP) standards.
Perform routine and specialized laboratory analyses (e.g., hematology, biochemistry, microbiology) as required by clinical trial protocols, ensuring accuracy and timeliness.
Accurately record test results and promptly report abnormal findings to the study team, ensuring timely data entry into clinical trial databases.
Ensuring timely dispatch of test results
Prepare and package biological samples for domestic and international shipment in compliance with IATA regulations and study-specific protocol requirement.
Ensure all laboratory procedures and documentation meet regulatory, ethical, and sponsor requirements, including proper handling of SOPs, logs, and deviation reports.
Maintain strict adherence to quality control procedures, calibration schedules, and equipment maintenance to ensure compliance with regulatory standards.
Monitor lab supplies and reagents, ensuring stock levels are adequate and that all materials are within expiration and validated for use.
Adhere to biosafety and infection control protocols to maintain a safe laboratory environment.
Participate in training sessions, internal audits, and continuous improvement initiatives to maintain laboratory excellence
Vacancy Requirements:
At least four (4) years of relevant work experience; Mandatory
Diploma in any of the following fields: Medical Laboratory Sciences, Laboratory sciences, Laboratory Technology, Medical Laboratory Technology or any other equivalent qualification from a recognized institution; Mandatory
Valid practicing license from the Kenya Medical Laboratory Technicians and Technologists Board, where applicable; Mandatory
At least three years’ experience working in a clinical trial or research setting will be an added advantage Added Advantage
Fulfil the requirements of Chapter Six of the Constitution. Mandatory