KENYA MEDICAL RESEARCH INSTITUTE (KEMRI)
CAREER OPPORTUNITIES – PRIME-KS STUDY
The Kenya Medical Research Institute (KEMRI) is a State Corporation established through the Science and Technology (Amendment) Act of 1979, mandated to conduct health research in Kenya. Over the years, KEMRI has built a team of more than 4,000 professionals across the country and continues to provide an enabling work environment that fosters growth, mentorship, and innovation. Ranked among Africa’s top research organizations, KEMRI is committed to advancing public health through cutting-edge research, scientific excellence, and technology-driven solutions.
KEMRI, in collaboration with Washington University in St. Louis (WUSTL), is implementing the PRIME-KS Study—“Precision Imaging to Evaluate Kaposi Sarcoma (PRIME-KS).” Funded by the National Institutes of Health (National Cancer Institute), this project aims to address oncology challenges in Kenya through the introduction of SkinScan3D, an innovative technology integrating liquid lens imaging and artificial intelligence for improved Kaposi Sarcoma assessment. The study plays a crucial role in supporting the integration of advanced technologies into clinical workflows, especially in low- and middle-income countries, where implementation science guides adoption, evaluation, and scale-up of novel health solutions.
To support the successful implementation of the PRIME-KS Study, KEMRI invites applications from qualified, motivated, and career-driven individuals to fill the following positions:
1. Study Doctor
Job Description:
The Study Doctor will be responsible for overseeing all clinical aspects of the PRIME-KS study, ensuring adherence to study protocols, and providing expert medical oversight during participant recruitment, screening, enrollment, and follow-up. The role involves clinical assessments of patients with Kaposi Sarcoma, interpretation of clinical findings, and coordination of medical evaluations aligned with study objectives. The incumbent will ensure participant safety, maintain accurate clinical documentation, and collaborate closely with study nurses, data managers, and principal investigators.
Key Responsibilities:
- Conduct participant clinical assessments, treatment, and follow-up evaluations.
- Provide clinical oversight to ensure compliance with Good Clinical Practice (GCP) standards.
- Review and verify participant medical data and case report forms for accuracy.
- Liaise with local health facilities and project partners to facilitate smooth study implementation.
- Support capacity building and mentorship of clinical and research staff within the study.
- Contribute to medical report preparation and dissemination of study results.
2. Data Manager
Job Description:
The Data Manager will manage all data-related aspects of the PRIME-KS study, ensuring data quality, integrity, and security. The role involves database setup, validation, cleaning, and continuous monitoring to guarantee reliable analysis and reporting. The incumbent will work closely with the research and clinical teams to ensure timely and accurate data entry, troubleshooting of data inconsistencies, and generation of progress reports.
Key Responsibilities:
- Design, test, and maintain the study database and related data collection systems.
- Perform data cleaning, validation, and quality assurance.
- Generate data summaries, reports, and statistical analyses as needed.
- Train research staff on data entry protocols and ensure compliance with study guidelines.
- Ensure confidentiality and protection of participant data in line with institutional ethics standards.
- Collaborate with investigators and statisticians to support data-driven decision-making.
3. Study Nurse
Job Description:
The Study Nurse will provide clinical and nursing support to study participants and play a pivotal role in the coordination of patient care within the PRIME-KS study. The incumbent will assist in participant recruitment, consent, clinical examination, specimen collection, and data documentation. The nurse will ensure adherence to study protocols and uphold high standards of ethical conduct and patient safety.
Key Responsibilities:
- Conduct participant screening, enrollment, and follow-up visits.
- Collect clinical samples and ensure accurate labeling and documentation.
- Maintain study participant files and ensure data accuracy and completeness.
- Monitor participants for adverse events and promptly report findings to the Study Doctor.
- Provide counseling, health education, and continuous support to participants.
- Assist in logistics, study coordination, and implementation of clinical procedures.
4. Research Assistant
Job Description:
The Research Assistant will support field and clinical research operations for the PRIME-KS study. The role involves participant recruitment, informed consent administration, data collection, and follow-up visits. The incumbent will work closely with clinical and data teams to ensure seamless coordination of research activities and adherence to ethical research standards.
Key Responsibilities:
- Conduct interviews and administer study questionnaires.
- Assist with participant follow-up and data collection in clinics and field sites.
- Ensure data entry accuracy and timely submission of study forms.
- Support quality control and verification of collected data.
- Assist in community engagement and sensitization activities.
- Maintain confidentiality and uphold participant rights throughout the study process.
5. Data Clerk
Job Description:
The Data Clerk will handle data entry and management of participant information gathered during the study. The role requires accuracy, confidentiality, and a strong commitment to data quality. The incumbent will work under the supervision of the Data Manager to ensure timely entry and validation of clinical and research data.
Key Responsibilities:
- Enter participant data into designated study databases and electronic systems.
- Perform routine verification to ensure data accuracy and completeness.
- Track and report data inconsistencies for correction and follow-up.
- Maintain organized filing systems for source documents and case report forms.
- Support data cleaning and compilation of reports for periodic review.
6. Driver
Job Description:
The Driver will be responsible for safe and timely transportation of study staff, materials, and participants. The role includes vehicle maintenance, compliance with traffic and safety regulations, and logistical support for study activities.
Key Responsibilities:
- Drive study vehicles to designated destinations as assigned.
- Ensure the safety of passengers and secure transport of study materials.
- Maintain vehicle cleanliness, fuel logs, and daily mileage records.
- Conduct routine vehicle checks and report mechanical issues promptly.
- Assist in logistical operations and delivery of research supplies.
7. Administration and Operations Coordinator
Job Description:
The Administration and Operations Coordinator will provide administrative, logistical, and operational support for the PRIME-KS study. The role involves coordinating procurement, budgeting, staff logistics, and communication between the study team and collaborating institutions. The incumbent will ensure efficient office management and facilitate smooth execution of project deliverables.
Key Responsibilities:
- Coordinate day-to-day administrative operations of the study.
- Oversee procurement, inventory management, and resource allocation.
- Support staff travel logistics, meeting coordination, and event planning.
- Maintain documentation related to project operations and finances.
- Facilitate communication among project partners, collaborators, and management.
- Ensure compliance with institutional administrative policies and procedures.
