KEMRI has built a strong professional team of over 4,000 employees deployed across the country. We have created a favorable work environment with able mentors who ensure talent is developed. We have also been ranked among the top Research organisations in Africa in research out put.
If you experience any delay in receiving an email notification at the end of the e-recruitment registration process, please refresh your email. In case of any challenge, please send your query to hr@kemri.go.ke
KEMRI does not charge any fee at any stage of the recruitment process (application, shortlisting, interviewing, and/or offer)
Biostatistician – Kisumu
Key Responsibilities:
- i. Perform cleaning, validation, and analysis of large, complex datasets from secondary sources such as demographic health surveys, surveillance systems, and other health research databases.
- ii. Review and validate data for completeness and perform logical checks to ensure timely query resolutions. Generate QC reports for review and clarification as well as a variety of other reports as required.
- iii. Apply statistical methods to analyze epidemiological, clinical, and survey data.
- iv. Use statistical software (R, Stata, or Python) to generate descriptive and inferential statistics.
- v. Contribute to the design and development of statistical models for specific research questions.
- vi. Prepare technical reports, summaries, and visualizations to communicate findings effectively.
Clinical Research Scientist – Kisumu & Siaya
Key Responsibilities:
- i. Implementing pre-clinical and clinical research projects and/or supervise designated aspects of the work;
- ii. General diagnosis, care, treatment and provision of specialized clinical care for study participants;
- iii. Assist in carrying out fieldwork and pre-clinical and clinical experimental procedures;
- iv. Carry out experimental and/or developmental work;
- v. Promote Good Clinical Practice in the conduct of the clinical trial by adhering to study protocol requirements, protecting rights and welfare of participants, assuring the integrity of data generated and directing the conduct of the clinical investigation according to regulations, SOPs and government guidelines;
- vi. Assess study participants and participate in medical decisions;
- vii. Prescribe medication for treatable medical conditions and monitor participants’ safety, manage, document, report and track adverse events;
- viii. Complete study specific CRFs/eCRFs and relevant study forms;
- ix. Conduct trial-related assessments and collection of data using case record forms in accordance to Good Clinical Practice (GCP);
- x. Write summary reports and maintain relevant records.
Medical Officer – Kisumu & Siaya
Key Responsibilities:
- i. Promote Good Clinical Practice in the conduct of the clinical trial by adhering to study protocol requirements, protecting rights and welfare of participants, assuring the integrity of data generated and directing the conduct of the clinical investigation according to regulations, SOPs and government guidelines;
- ii. Provide leadership, training, mentoring and guidance to clinical staff in all aspects of clinical trial;
- iii. Assess study participants and participate in medical decisions;
- iv. Prescribe medication for treatable medical conditions and monitor participants’ safety, manage, document, report and track adverse events;
- v. Complete study specific CRFs/eCRFs and relevant study forms;
- vi. Respond to monitor and data management team queries;
- vii. Scrutinize and interpret laboratory results;
- viii. Follow up research participants for study end points;
- ix. Conduct trial-related assessments and collection of data using case record forms in accordance to Good Clinical Practice (GCP);
- x. Write summary reports and maintain relevant records.
Senior Health Economist – Kisumu
Key Responsibilities:
- i. Undertake high quality research and contribute to peer-reviewed publications;
- ii. Co-design data collection tools for health facilities as well as staff and equipment surveys;
- iii. Plan and conduct the collection of economic and financial data, for the cost-effectiveness, budget impact, and equity analysis of PDMC;
- iv. Provide training support and supervision to fieldworkers involved in data collection;
- v. Coordinate with researchers involved in the qualitative research (feasibility, acceptability) to ensure that, where necessary, relevant financial and economic data is collected through key informant interviews (KII);
- vi. Analyse the economic and financial data, for the cost-effectiveness, budget impact and equity analysis of PDMC and to write up the findings for research reports, policy briefs, conference presentations and peer-reviewed journals;
- vii. Submit, attend and present (online or in presence) the results of the economic evaluation of PDMC at national and international conferences on health economics, child health and/or malaria;
Senior Research Administrator – Kisumu
Key Responsibilities:
- i. Lead preparation of all research documents including protocols, tools, regulatory materials, logs;
- ii. Chair research management meetings and provide regular project updates to project PI and co-investigators
- iii. Conduct performance appraisal of study site staff in liaison with the relevant technical supervisors of the staff members in Kenya.
- iv. Develop standard operating procedures (SOPs) for all data collection and participant interactions, including for safeguarding;
- v. Organize and lead local research management meetings, and present study updates as necessary;
- vi. Present findings at national and international seminars and conferences;
- vii. Lead in writing reports and manuscripts in close collaboration with LSTM and other partners.
- viii. Ensure compliance with ethical research standards and safeguarding protocols;
- ix. Compile and lead submission on documents for Kenyan Poisons and Pharmacy Board;
- x. Conduct regular safeguarding reviews and implement corrective measures.
End-Point Research Assistants – Suba, Mbita, Rongo
Key Responsibilities:
- i. Gaining a thorough understanding of the study design and objectives to ensure the successful implementation of study activities in strict compliance with the study protocol.
- ii. Establishing rapport with potential and enrolled study participants and introducing the study to them.
- iii. Conducting recruitment, screening, and obtaining informed consent from participants.
- iv. Collaborating with Community Health Promoters (CHPs) to navigate study communities and conduct population censuses and household enumerations.
- v. Uploading and backing up data collected using study tablet computers daily.
- vi. Measuring participants’ health metrics, such as blood pressure, height, and weight, as directed.
- vii. Providing comprehensive HIV testing services, including pre-test counseling, conducting rapid HIV tests, post-test counseling, and referring participants as appropriate based on test outcomes.
- viii. Performing phlebotomy and collecting blood samples from participants.
- ix. Offering support and information to study participants as needed.
- x. Tracing participants, filing, and maintaining accurate study documents.
- xi. Entering data in real-time into the Open MRS system and assisting with correcting frequent data errors identified by the data coordinator.
- xii. Ensuring proper documentation in all study Case Report Forms (CRFs) and Ministry of Health (MOH) forms and registers.
- xiii. Performing other duties as assigned by study coordinators.
- xiv. Generating weekly retention reports and sharing them with the Retention Coordinator.
- xv. Sending appointment reminders to study participants.
Research Assistants – Migori
Key Responsibilities:
- Implement research protocols and Standard Operating Procedures (SOPs).
- Recruit participants at schools and obtain informed consent from adolescents and caregivers.
- Conduct follow-ups with participants via phone or in person.
- Perform participant screening, quantitative interviews (using REDCap), and in-depth interviews.
- Collect, abstract, and manage data (e.g., report cards, anthropometric measurements).
- Ensure accurate data entry in collaboration with the Data Manager and Study Coordinator.
- Maintain detailed records of research activities.
Study Administrator – Finance/Operations – Migori
Key Responsibilities:
- Manage petty cash, process vouchers, and reconcile bank transactions using QuickBooks.
- Prepare donor financial reports, budget vs expenditure reports, and cash flow projections.
- Oversee procurement plans and vendor management.
- Assist in training logistics, conferences, and transport scheduling.
- Review and approve operational invoices.
Lay Mental Health Workers – Migori
Key Responsibilities:
- Conduct community outreach and provide psychosocial support to adolescents and their caregivers.
- Facilitate workshops on relationship building, communication, and stress management.
- Deliver culturally sensitive mental health guidance.
- Collect data to evaluate the project’s mental health components.
Driver – Migori
Key Responsibilities:
- Conduct community outreach and provide psychosocial support to adolescents and their caregivers.
- Facilitate workshops on relationship building, communication, and stress management.
- Deliver culturally sensitive mental health guidance.
- Collect data to evaluate the project’s mental health components.
