AddressKenya Medical Research Institute, Off Mbagathi Way Nairobi
About Kenya Medical Research - KEMRI
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 r... read moreesearch in Kenya.
Key Responsibilities:
Design and implement testing procedures for specimens received as part of disease outbreak investigations in the country and the region
Design and implement testing proce
Key Responsibilities:
Assist in receipt and processing of biological samples, storage and shipment of samples
Preparation of laboratory reagents
Ensure all specimens and request forms are ac
Key Responsibilities:
Support the implementation and coordination of fellowship programs, leadership development initiatives, research training programs, and innovation ecosystem activities.
C
Key Responsibilities:
Design and oversee statistical analysis plans, study designs, sample size calculations, and advanced analytical methodologies for CHAMPS and related studies.
Build, valid
Key Responsibilities:
Develop Independent Development Plans (IDPs) within the first three months, outlining a professional career trajectory and pathway to becoming an independent scientist.
C
Key Responsibilities:
Assist in reception, labeling, processing, storage, and transport of biological specimens according to study protocols and SOPs
Support preparation of laboratory reagents
Key Responsibilities:
Assisting in the accurate entry of study data into electronic databases and data capture system
Supporting verification of data completeness, consistency, and accuracy in
Key Responsibilities:
Day-to-day office administrative and operational activities
Filing, organization, archiving, and retrieval of study documents and administrative records
Preparation, ph
Key Responsibilities:
Collection of accurate information from the study participants in line with the standards and guidelines set in the study protocol
Schedule and prepare a work plan of fol
Key Responsibilities:
Collection of accurate information from the study participants in line with the standards and guidelines set in the study protocol
Schedule and prepare a work plan of fol
Key Responsibilities:
Collection of accurate information from the study participants in line with the standards and guidelines set in the study protocol
Schedule and prepare a work plan of fol
Key Responsibilities:
Collection of accurate information from the study participants in line with the standards and guidelines set in the study protocol
Schedule and prepare a work plan of fol
Key Responsibilities:
Morning and afternoon charting of the Investigational Product (IP) room temperatures
Shipment of IPs as requested.
Receiving and storage of the IPs at the IP room
Ens
Key Responsibilities:
Morning and afternoon charting of the Investigational Product (IP) room temperatures
Shipment of IPs as requested.
Receiving and storage of the IPs at the IP room
Ens
Key Responsibilities:
Primary responsibility is to assist the site Data Manager in Data management of all studies.
Assist in the design and implementation of SOPs, CRFs and Databases.
Suppor
Key Responsibilities:
Primary responsibility is to assist the site Data Manager in Data management of all studies.
Assist in the design and implementation of SOPs, CRFs and Databases.
Suppor
Key Responsibilities:
Screen, consent, and enroll study participants who meet eligibility criteria, ensuring full adherence to ethical standards and study protocols.
Conduct baseline and follo
Key Responsibilities:
Screen, consent, and enroll study participants who meet eligibility criteria, ensuring full adherence to ethical standards and study protocols.
Conduct baseline and follo
