There are exciting jobs open at Kemri with application deadlines fast approaching. Grab your chance now by applying for the following positions at K
There are exciting jobs open at Kemri with application deadlines fast approaching. Grab your chance now by applying for the following positions at Kemri. Link at the down end of the page takes you to the KEMRI website where you can apply.
The Kenya Medical Research Institute (KEMRI)
About us
The Kenya Medical Research Institute (KEMRI) is a State Corporation established in Kenya in 1979 through the Science and Technology (Repealed) Act, Cap 250 of the Laws of Kenya operated under the Science Technology and Innovation Act, 2013 as the national body responsible for carrying out research in human health in Kenya. Currently, KEMRI operates under Legal Notice No. 35 of March 2021
KEMRI has grown from its humble beginning over 40 years ago to become a regional leader in human health research.
The Institute currently ranks as one of the leading Centres of excellence in health research both in Africa as well as globally.
Background Information
The PRIME-KS study, titled “Precision Imaging to Evaluate Kaposi Sarcoma (PRIME-KS),” is being implemented by the Kenya Medical Research Institute and funded by the National Institutes of Health (National Cancer Institute) through Washington University in St. Louis (WUSTL). The study aims to address oncology challenges in Kenya through the introduction of SkinScan3D, an innovative technology that integrates liquid lens imaging and artificial intelligence for improved Kaposi Sarcoma assessment. This project plays a crucial role in supporting integration of advanced technologies into clinical workflows in low- and middle-income countries, where implementation science is essential to guide adoption,
evaluation, and scale-up.
The project has the following vacancies:
I. Position: Study Doctor ( 1 Position) K MR/ 5
Reports to: Principal Investigator
Location: KISUMU
Duration: 1 year Renewable Contract, subject to availability of funds
Duties and Responsibilities:
- Collect, verify, and accurately document demographic, clinical, and lesion measurement data (including SOC ruler-based ACTG criteria and SS3D imaging).
- Implement and lead phased adoption of SS3D-supported lesion measurement, including provider training and transition from SOC-only measurement.
- Train and mentor clinical staff on ACTG protocols, SS3D use, and clinical research best practices to ensure protocol adherence and data integrity.
- Ensure participant safety, identify and manage adverse events, and coordinate with safety oversight bodies.
- Oversee day-to-day study operations, including initiation, execution, workflow optimization, direct observation, and time-motion studies.
- Manage data quality, including supervision of data collection and entry, accuracy checks, and quality control procedures.
- Coordinate communication across investigators, clinical teams, external partners, and stakeholders to support implementation and dissemination.
- Lead program evaluation activities, including usability, acceptability, feasibility assessments, and micro-costing.
- Support research funding and scientific output through grant writing, manuscript development, and reporting to funders and regulators, plus presenting findings.
- Oversee budget and resource management, including equipment procurement, expenditure tracking, and financial reporting.
Required Qualifications:
- MBChB or equivalent medical degree with a valid practising license
- Master’s degree in Public Health (MPH) or a relevant field (e.g., Epidemiology, Global Health, Clinical Research will be an added advantage
- At least 2 years of demonstrated research experience in Clinical or implementation studies, preferably in HIV, oncology, or infectious diseases. Ability to write, review, and contribute to grant applications and secure research funding.
II. Position: Data Manager ( 1 Position) K MR/ 5
Reports to: Study Doctor
Location: KISUMU
Duration: 1 year Renewable Contract, subject to availability of funds
Duties and Responsibilities:
- Develop, implement, and ensure adherence to study protocols, SOPs, and data management plans
- Oversee data collection, entry, cleaning, validation, and secure storage to maintain data accuracy, completeness, and integrity.
- Conduct routine data quality checks, audits, and generate QC reports to ensure timely correction of discrepancies.
- Develop, review, and maintain data collection tools and databases (e.g., ODK, Excel, Epi Info, REDCap, web and mobile solutions).
- Build capacity of Data Officers and train study teams on data systems, tools, and tracking logs to ensure consistent and high-quality data capture.
- Support setup and maintenance of data-related hardware, network systems, and real-time transmission solutions.
- Ensure compliance with the Data Protection Act and Institution data governance policies, including confidentiality, backups, security, and restricted access
- Generate dashboards, statistical analyses, and visual reports (Power BI, Tableau, Excel) to support monitoring, evaluation, and evidence-based decision-making.
- Prepare and submit timely monitoring reports (daily to quarterly, DSMB, sponsor) in line with reporting schedules.
- Attend to ad hoc data requests and perform additional assigned duties to support project data needs.
Required Qualifications:
- Bachelor’s Degree in Computer Science, Data Science, Epidemiology, Biostatistics, Applied Statistics or any other relevant field from a recognized institution.
- Master’s Degree in the relevant field
- Epidermiological and statistical analysis skills using tools such as SAS, STATA, R, Python, or similar. Conversant with data management databases i.e. MS access, Excel SQL or Visual basics. Proficiency in REDCap programming and customization.
III. Position: Study Nurse ( 1 Position) K MR/ 5
Reports to: Study Doctor
Location: KISUMU
Duration: 1 year Renewable Contract, subject to availability of funds
Duties and Responsibilities:
- Screen, consent, enroll, and follow up study participants, ensuring accurate documentation of clinical procedures, adverse events, and visit outcomes.
- Provide study information, address participant questions, and support retention through scheduled clinical assessments and follow-up coordination.
- Assist with lesion measurements, skin biopsy procedures, and safe handling of biological samples per protocol and SOPs.
- Label, package, transport, and track samples, coordinating closely with KEMRI and Washington University laboratories for receipt, storage, and shipment documentation.
- Record participant data in CRFs and study databases accurately and promptly, ensuring data quality through collaboration with the Data Manager.
- Maintain secure, organized clinical and research records in compliance with protocol requirements.
- Support qualitative research activities, including planning, recruitment, transcription, and secure data handling.
- Participate in study operations with the clinical and data management team, providing weekly progress updates on recruitment, follow-up, and data entry.
- Assist in resource management including supply procurement, inventory control, and basic financial/budget tracking.
- Prepare and submit regulatory documents to relevant ethics and oversight bodies, including amendments, safety reports, and deviations.
Required Qualifications:
i. Bachelor’s Degree in Nursing
ii. Master’s in public health, Nursing and related courses is an added advantage
iii. Minimum of 2–3 years of research experience in research settings or clinical trials is highly
desirable
IV. Position: Research Assistant ( 1 Position) K MR/ 7
Reports to: Study Doctor
Location: KISUMU
Duration: 1 year Renewable Contract, subject to availability of funds
Duties and Responsibilities:
- Identify, mobilize, screen, consent, and enroll eligible participants while providing clear study information and appointment reminders.
- Trace and re-engage participants who miss visits or are lost to follow-up through home visits, phone calls, community outreach, and motorbike tracing where necessary.
- Maintain accurate and secure records of participant contact, follow-up outcomes, and retention activities in line with study protocols.
- Build strong, trust-based relationships with participants and community stakeholders to support engagement and retention.
- Collaborate with the study team to identify and address barriers to retention using culturally sensitive and ethical approaches.
- Coordinate qualitative research activities including planning, recruitment, logistics, consenting, and facilitation of interviews/FGDs.
- Transcribe, manage, and analyze qualitative data using tools such as NVivo, Atlas.ti, or Dedoose while ensuring confidentiality and proper storage.
- Prepare reports, summaries, and dissemination outputs such as abstracts, presentations, and manuscript contributions.
- Accurately enter clinical and research data into systems (e.g., REDCap), complete CRFs, and support database reporting.Assist with field logistics, supply management, and provide regular updates on recruitment, retention, and data activities during team meetings.
Required Qualifications:
- Diploma in Community Health, Social Work, Community Development or any other related Diploma in Social Sciences.
- Bachelor’s Degree in the above fields will be an added advantage
- Excellent verbal and written communication skills, high level computer and internet skills with daily access to internet
V. Position: Data Clerk ( 1 Position) K MR/ 8
Reports to: Data Manager
Location: KISUMU
Duration: 1 year Renewable Contract, subject to availability of funds
Duties and Responsibilities:
- Accurately enter participant information and clinical/research data into electronic systems such as ODK, OpenMRS, and REDCap.
- Maintain organized participant files, source documents, CRFs, and results in compliance with study protocols.
- Conduct routine data cleaning, validation, and discrepancy resolution to ensure data quality and integrity.
- Perform regular data backups and ensure secure storage of all study records.
- Cross-check data against source documents and prepare materials for monitoring visits and audits.
- Generate routine data summaries, tracking logs, and progress reports to support study operations.
- Collaborate with clinical and field teams to reconcile data and provide updates during study meetings.
- Provide general data-related support as assigned to ensure smooth and timely study implementation.
Required Qualifications:
- Diploma in Health Records and Information or equivalent training.
- Previous experience in data entry or records management in a healthcare or research setting preferred.
- Basic computer literacy and proficiency in Microsoft Office (Word, Excel) and data entry platforms (ODK, OpenMRS, Redcap).
- Ability to maintain confidentiality of participant information. Good communication and teamwork skills
VI. Position: Driver ( 1 Position) K MR/ 8
Reports to: Study Administrator
Location: KISUMU
Duration: 1 year Renewable Contract, subject to availability of funds
Duties and Responsibilities:
i. Safely transport staff, participants, and study materials while complying with all road safety regulations.
ii. Conduct routine vehicle checks, maintain logbooks, and report any mechanical issues for timely servicing and repairs.
iii. Ensure the security of passengers, equipment, and study cargo at all times.
iv. Deliver and collect study documents, parcels, supplies, and support logistics for field activities.
v. Assist with office administrative tasks such as photocopying, scanning, filing, and basic supervised data entry.
vi. Support organization of participant files, records, and materials for meetings and trainings.
vii. Perform other duties as assigned to ensure smooth daily study operations.
Required Qualifications:
- ‘O’ Level school Certificate Grade D (Plus)
- Valid driving license class BCE
- Certificate of Good Conduct
- Certificate of defensive Driving Course
Required Experience:
- Good communication skills
- Basic computer literacy
- Ability to work with minimum supervision and under pressure
VII. Position: Administration and Operations Coordinator, 1 Position) K MR/ 5
Reports to: Program Fiscal Manager
Location: KISUMU
Duration: 1 year Renewable Contract, subject to availability of funds
Duties and Responsibilities:
- Manage calendars, meetings, and calls
- Coordinate with U.S.based collaborators
- Anticipate project needs and ensure priorities are well-prepared
- Organize local travel logistics and prepare itineraries
- Draft, edit, and manage correspondence, presentations, and reports
- Support with academic writing tasks (bonus skill)
- Maintain accurate records and organize documents
- Ability to use AI and digital tools to streamline administrative tasks
- Travel occasionally between Kisumu and Nairobi
- Assist with social media and online presence
- Coordinate scheduling, communication, and travel.
Required Qualifications:
- Bachelors of Commerce Degree in Business Administration, Finance/ Accounting or equivalent
- Detail-oriented, highly organized, and able to thrive in a fast-paced, cross-cultural environment.
- Excellent Communication Skills
- Highly organized, detail-oriented, and able to work independently
- Highly Proficient in Microsoft Office and open to AI and new tools
- Discreet, reliable, and adaptable
- Experience in academic writing or social media management
NOTE
1. Successful candidates will be required to provide the following:
- Certificate of good conduct,
- HigherEducation Loans Board compliance certificate,
- KRA Tax compliance certificate,
- Credit Reference Bureau clearance certificate, and
- Ethics and Anti-Corruption Commission clearance.
2. Kindly attach your CV, cover letter, copies of certified academic and professional certificates, testimonials and other relevant documents.
3. All the applications to be done through KEMRI Website https://www.kemri.go.ke/ e- recruitment -E Recruitment Portal on or before 30th November, 2025 latest 5.00 p.m.
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