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 develop data entry forms and surveys using REDCap to ensure efficient and accurate data collection.
Implement branching logic, skip patterns, and validation ch
Key Responsibilities:
Work with the programs Finance manager/KEMRI supply chain officers to establish contracts and Pricing and ensuring proper maintenance and serving as primary liaison with ut
Key Responsibilities:
Plan, manage, and supervise the day-to-day operations of the study ;
Supervise the study teams (Research Assistants and Data Analyst) to ensure that the study is conducte
Key Responsibilities:
Manage study setup, participant recruitment, and field activities across multiple sites.
Oversee regulatory compliance, including obtaining protocol submissions to CSC an
Key Responsibilities:
Recruitment and consenting of potential study participants;
HIV counseling and testing of potential study participants;
Taking vital signs during scheduled study visits
Key Responsibilities:
Sample collection and processing including culture, identification and antimicrobial susceptibility testing;
Media preparation and quality control (QC);
Routine laborat
Key Responsibilities:
Assist in the implementation of research projects and supervising designated aspects of the project.
Assist in training research assistants and screeners
Assist in carr
Key Responsibilities:
Assist in the implementation of research projects and supervising designated aspects of the project.
Assist in training research assistants and screeners
Assist in carr
Key Responsibilities:
Coordination of the activities that facilitate the efficient management of the of the program, the team and its operations
Organizing and managing The Director’s ca
Key Responsibilities:
Performing Clinical Assessments.
Collecting specimens.
Conducting interviews, administering Case report forms, and form completion
Offer support counselling to study
Key Responsibilities:
Administer respective Case Report Forms (CRFs)
Carrying out QA/QC of study CRFs and source docs and resolve queries that may arise.
Dispensing drugs and Study products
Key Responsibilities:
Coordinate all issues related to investigational products importations, supply and preparation of all doses for administration/use to/by the study participants.
Maintaini
Key Responsibilities:
Provide strategic leadership in accordance with the mandate of the KEMRI;
Official spokesperson of the organization and responsible for stakeholder management and the enh
Key Responsibilities:
Provide strategic leadership in accordance with the mandate of the KEMRI;
Official spokesperson of the organization and responsible for stakeholder management and the enh
Key Responsibilities:
Provide strategic leadership in accordance with the mandate of the KEMRI;
Official spokesperson of the organization and responsible for stakeholder management and the enh
Key Responsibilities:
Provide strategic leadership in accordance with the mandate of the KEMRI;
Official spokesperson of the organization and responsible for stakeholder management and the enh
Key Responsibilities:
Work closely with the trial Principal Investigators (PIs) and the site Study Coordinator to set up and execute a clinical trial [one position is for a phase 2 clinical tria
Key Responsibilities:
Ensure that the clinical trial is conducted in compliance with the approved protocol, GCP, and applicable regulatory requirements at the site level.
Monitor the implement
