Internship | Job Vacancies at Kenya Medical Research Institute (KEMRI)

Job Vacancies at Kenya Medical Research Institute (KEMRI)

Pharmaceutical Technologist – Kisumu at Kenya Medical Research – KEMRI

Key Responsibilities:

  • Dispensing prescribed medications and pharmaceutical preparations
  • Verifying and maintaining information relating to patients
  • Ordering and recording of drugs and other supplies;
  • Verifying and maintaining records relating to patients;
  • Custody and storing of drugs;
  • Ensuring that the working environment meets the stipulated requirements
  • Prepare pharmacy/drugs monthly reports

Vacancy Requirements:

  • Diploma in Pharmaceutical Technology or its equivalent from a recognized institution;    Mandatory
  • Registration Certificate issued by the Pharmacy and Poisons board;    Mandatory 
  • Good Clinical Practice (GCP) and Good Pharmacy Practice (GPP) – Added advantage    Added Advantage
  • Proficiency in computer application    Mandatory
  • Communication skills    Mandatory
  • Interpersonal skills    Mandatory
  • Team player    Mandatory

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Assistant Coordinators – Nairobi at Kenya Medical Research – KEMRI

Key Responsibilities:

  • Assist in the development and implementation of standard operating procedures (SOPs) for all study procedures
  • Create training schedules for the study, track and create reports on outcomes of all training and maintain training records for the company.
  • Establishing strategic partnerships with the relevant stakeholders for research, training, innovations and technology
  • Monitoring and evaluating implementation of the study
  • Support in Writing manuscripts, reports and translating research findings
  • Assist in the disseminating and translating research findings for evidence-based policy formulations and implementation
  • Assist in planning and coordination of meetings for both internal project staff and external collaborators
  • Host/participate in scheduled conference calls with the international study partners.
  • Participate in development of research proposals in the relevant research thematic area
  • Conduct participants trainings
  • Gather and evaluate information from participants and management on previous training to identify weaknesses and areas that need additional training.
  • Inform participants on scheduled training and track their progress.
  • Recommend training materials and methods, order and maintain training equipment and facilities and manage the budget set for training
  • Any other relevant duties as assigned by the supervisor

Vacancy Requirements:

  • Bachelor of Medicine and Bachelor of Surgery    Mandatory
  • Masters of Medicine, Masters of Public Health or equivalent will be added advantage    Added Advantage
  • Experience in women’s health -obgyn / adolescents -women and children’s health preferable    Mandatory
  • Training in education/ curriculum development/ strategy / project and program implementation desirable    Desirable

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Procurement Officer – Nairobi at Kenya Medical Research – KEMRI

Key Responsibilities:

  • Assist in the selection of appropriate suppliers and contractors, to promote good procurement practice with due regard to sustainability, ethical purchasing standards and costing
  • Draft an appropriate service level agreement to properly evaluate the performance of suppliers, and report on this on a regular basis.
  • Work with departmental heads to determine procurement needs, quality and delivery requirements.
  • Responsible for order placement timing, supply / demand alignment, material replenishment and supplier performance
  • Maintain contracts with vendors
  • Review inventory and update as required
  • Receive orders from various departments
  • Initiate and keep track of orders
  • Receive, inspect and distribute orders
  • Reconcile or resolve order discrepancies with supplies.
  • Monitor delivery times to ensure they are on time
  • Any other relevant duties as assigned by the supervisor

Vacancy Requirements:

  • Bachelor Degree in supply chain management or a procurement related degree    Mandatory
  • Previous experience as a Procurement Officer, or similar role    Desirable
  • Computer literacy qualification is essential.    Desirable
  • Proven ability to utilize and develop computerized spreadsheets and word processing applications    Desirable
  • Procurement Software and Asset Software experience is essential.    Desirable
  • Independent self-starter with attention to detail    Desirable
  • Possesses integrity and ability to maintain accurate and confidential records    Desirable

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Psychiatric Nurses – Kisumu – 3 Posts at Kenya Medical Research – KEMRI

Key Responsibilities:

  • Develop, review and adhere to the study standard operating procedures (SOPs)
  • Sensitize the community/health facilities teams on the study.
  • Respond to questions about the study posed by participants and the community in consultation with the study coordinator.
  • Screen and enroll study participants and Administer Informed Consent administration per study protocol.
  • Administer study questionnaires as per protocol, accurately record the data and perform quality checks before submitting the data.
  • Maintain documentation of all study activities as per study standard operating procedures.
  • Participate in multidisciplinary case reviews for PPWH who do not respond to intervention.
  • Provide appropriate referral for non-intervention study participants with high CMD scores per protocol.
  • Follow-up participants to ensure study visits are conducted in a timely manner.
  • For study participants on medication, monitor and update the psychiatrist and MDT on progress.
  • Ensure participant retention and adhere to site retention strategies.
  • Interact with participants in accordance with ethical standards and guidelines for research involving human subjects. This includes safeguarding participants’ confidentiality, respecting their autonomy, and protecting their well-being
  • Prepare daily updates, weekly and monthly progress reports, adverse event reports, serious adverse event reports as required.
  • Provide supervision to mentor mothers to ensure implementation of the interventions and attend all study related meetings.
  • Collaborate closely with other members of the research team-Behavioural Care officers, Mentor mothers, data team, principal investigators, health facility staff, and larger Kargeno-research Hub staff.
  • Any other duties as assigned by the supervisor.

Vacancy Requirements:

  • Diploma in Nursing (KRCHN) from an accredited institution.    Mandatory
  • Current licensure as a registered nurse (RN) in the relevant jurisdiction.    Mandatory
  • Certified training in psychiatry from an accredited institution.    Mandatory
  • Experience working in psychiatric or mental health settings, preferably in a research capacity.    Mandatory
  • Strong knowledge of psychiatric disorders, assessment tools, and evidence-based treatments.    Mandatory
  • Excellent interpersonal and communication skills, with the ability to collaborate effectively in a team environment.    Mandatory
  • Attention to detail, organization, and time management skills.    Skills & Competencies
  • Commitment to ethical conduct and compliance with regulatory requirements in research.    Skills & Competencies
  • Strong analytical ability, planning, and organizational skills    Skills & Competencies
  • Excellent verbal and written communication skills.    Skills & Competencies
  • Ability to work with multi-skilled teams.    Skills & Competencies
  • Analytical and report writing skills    Skills & Competencies

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Behavioral Care Manager – Kisumu – 3 Posts at Kenya Medical Research – KEMRI

Key Responsibilities:

  • Develop, review and adhere to the study standard operating procedures (SOPs).
  • Sensitize the community/health facilities teams on the study- Provide health education on PMTCT, stigma, IPV, and CMD self-care to participants.
  • Respond to questions about the study posed by participants and the community in consultation with the study coordinator.
  • Screen and enroll study participants and Administer Informed Consent administration per study protocol.
  • Administer study questionnaires as per protocol, accurately record the data and perform quality checks before submitting the data.
  • Use the Decision Support Electronic Health Record (DSEHR) system to prioritize participant care and monitor participants’ progress throughout the study.
  • Lead the multidisciplinary team (MDT) case reviews for study participants and keep the MDT team up to date on participant progress.
  • Lead the Virtual Psychiatric review process for referred participants- by planning with the psychiatrist for the review of participants and presenting the case during the Virtual psychiatrist review.
  • Provide support to mentor mothers to deliver PM+ intervention to participants as per study protocol.
  • Interact with participants in accordance with ethical standards and guidelines for research involving human subjects. This includes safeguarding participants’ confidentiality, respecting their autonomy, and protecting their well-being
  • Collaborate closely with other members of the research team-Psychiatric nurses, Mentor mothers, data team, principal investigators, health facility staff, and larger Kargeno-research Hub staff.
  • Attend weekly study meetings and Prepare and share reports on the progress of the intervention.
  • Perform any additional duties as assigned by the supervisor.

Vacancy Requirements:

  • Bachelor’s degree in sociology, psychology, anthropology or a related field from a recognized institution.    Mandatory
  • Previous experience working with people living with HIV/AIDS (PLWHA) is essential.    Mandatory
  • Registered with relevant professional body.    Mandatory
  • Candidates should demonstrate proficiency in data entry and management.    Mandatory
  • Training in behavioral health management is an added advantage.    Added Advantage
  • Good communication skills, both verbal and written.    Mandatory
  •  Ability to work collaboratively in a multidisciplinary team setting.    Mandatory
  • Strong organizational skills and attention to detail.    Mandatory
  • Flexibility and adaptability to work in a fast-paced environment.    Mandatory
  • Empathetic and compassionate approach to patient care.    Desirable
  • Ability to maintain confidentiality and respect patient privacy.    Desirable
  • Cultural competence and sensitivity to diverse patient populations.    Desirable
  • Problem-solving skills and ability to think critically.    Desirable
  • Commitment to continuous professional development and learning.    Desirable
  • Experience working with electronic health records systems is an advantage.    Desirable
  • Familiarity with evidence-based practices in behavioral health management.    Desirable
  • Capacity to thrive in a dynamic and evolving healthcare environment.    Desirable

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Data Manager – Kisumu at Kenya Medical Research – KEMRI

Key Responsibilities:

  • Read and understand the study protocol, and develop, review, and ensure adherence to study standard operating procedures (SOPs) in line with protocol requirements
  • Develop and implement data management plans to ensure data accuracy, completeness, and integrity by strengthening data quality systems through routinely conducting data validation checks to flag out data queries and entry errors, thereby fostering concurrence and accuracy across all data collection and reporting systems
  • Perform data quality checks and generate QC reports to enable prompt correction of discrepancies and Oversee data collection, cleaning, validation, and storage to ensure the accuracy and completeness of study data
  • Plan, organize, and perform data quality audits; coordinate data cleaning through monitoring and evaluation activities; and verify data accuracy prior to the submission of all data reports
  • Build the capacity of Data Officers to effectively manage and respond to various project data demands with competence and efficiency
  • Train the study team on data collection tools, study tracking logs, and the use of the study database to ensure accurate and consistent data capture
  • Design, develop, review, and maintain routine and ad hoc data collection tools including data entry forms, surveys, ODK, Excel, Epi Info, REDCap, and other databases to ensure efficient and accurate data capture
  • Design, develop, and implement web-based and mobile health solutions to facilitate real-time data transmission, reporting, and information sharing
  • Support the setup and maintenance of data-related hardware and network systems to ensure seamless data access, storage, and transmission
  • Develop and implement project data mining scripts to automate data accuracy checks and generate reports on identified inconsistencies
  • Ensure the monthly Performance Monitoring Plan (PMP) and performance dashboards are well-developed and aligned with project needs and integrated into the Decision Support and Electronic Health Records (DSEHR) system to enhance data-driven decision-making
  • Establish and maintain a secure, organized database for longitudinal cohort study data to support accurate storage and retrieval of patient and project information.
  • Ensure all data storage and handling practices comply with the Data Protection Act, 2019, including data confidentiality, restricted access, and proper documentation from the onset of data entry and storage
  • Ensure project data and all related documents are securely stored in the designated physical or electronic repository mechanisms in accordance with organizational data governance policies
  • Regularly update and back up the study database to prevent data loss and ensure continuous availability and integrity of data
  • Prepare reports, dashboards, and visual summaries of project results using Power BI, Excel, Tableau, and other data visualization tools, and perform statistical analyses to derive meaningful insights from longitudinal data
  • Ensure timely and accurate preparation and submission of project monitoring reports, including daily, weekly, monthly, quarterly, Data Safety Monitoring Board (DSMB), and sponsor reports, in alignment with reporting schedules and sponsor requirements
  • Assist in the preparation of data summary slides and visual presentations for donors and project team meetings to support evidence-based discussions and decision-making
  • Ensure compliance with regulatory requirements and ethical standards for data management and Attend to ad hoc data requests as may arise from time to time
  • Collaborate with other members of the research team- Behavioral Care officers, Mentor mothers, Psychiatric nurses, data team, principal investigators, health facility staff, and larger Kargeno-research Hub staff
  • Perform any other relevant duties as may be assigned from time to time to support project objectives and data management functions

Vacancy Requirements:

  • Bachelor’s Degree in Computer Science, Biostatistics or Applied Statistics or any other related field from a recognized institution    Mandatory
  • Two years’ experience in working with Electronic Health Record (EHR) Systems    Mandatory
  • Experience using digital data collection platform    Mandatory
  • Training in statistical packages/programs, preferably STATA, Excel, R and Python and statistical analysis will be an added advantage    Added Advantage
  • High level of competency in using Microsoft, Excel, Word and PowerPoint.    Skills & Competencies
  • Analytical and report writing skills    Skills & Competencies
  • Presentation skills and a good Team player    Skills & Competencies
  • Excellent organizational skills, Written |& verbal communication skills , attention to detail and focus on quality and innovation.    Skills & Competencies

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Exciting Career Opportunities at KEMRI

The Kenya Medical Research Institute (KEMRI) is seeking passionate and dedicated professionals to join its dynamic team in advancing cutting-edge research and public health solutions. We have a range of openings — from early post-doctoral researchers to community trackers — across various locations including Kilifi and Kisumu. These roles offer a unique opportunity to contribute to impactful research projects in genomics, bioinformatics, serosurveillance, and more.

(Click the blue job Titles to access the job descriptions)

Reference

Job Title/Designation

Employment
Type

Posts

Application Deadline

VN00851

Early Post-Doctoral Mathematics Modeller – Kilifi

Contract

1

08/12/25: 5:00:00 PM

VN00852

PhD Studentship – KEMRI CGHR Kisumu

Internship

1

08/26/25: 5:00:00 PM

VN00853

Community Tracker – Kisumu

Contract

6

08/26/25: 5:00:00 PM

VN00854

Early Post Doctoral Researcher -Yellow Fever

Contract

1

08/24/25: 5:00:00 PM

VN00855

Assistant Research Officer -Genomics and Bioinformatics

Contract

1

08/24/25: 5:00:00 PM

VN00856

Early Post-Doctoral Researcher – Serosurveillance

Contract

1

08/24/25: 5:00:00 PM

VN00857

Early Post-Doctoral Researcher

Contract

1

08/24/25: 5:00:00 PM


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