Clinical Officer
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KEMRI is recruiting a Clinical Officer to support clinical research activities in Thika. The role involves participant screening, enrolment, follow-up, clinical care, data collection, and counselling within cervical cancer prevention and HIV care research programmes. Applications are due by 15th November 2026.
- Clinical Officer role supporting research and patient care
- Work on cervical cancer prevention and HIV programmes
- Based in Thika under KEMRI
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KEMRI is recruiting a Clinical Officer to support clinical research activities in Thika. The role involves participant screening, enrolment, follow-up, clinical care, data collection, and counselling within cervical cancer prevention and HIV care research programmes. Applications are due by 15th November 2026.
- Clinical Officer role supporting research and patient care
- Work on cervical cancer prevention and HIV programmes
- Based in Thika under KEMRI
- Deadline: 15th November 2026
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Not enough public dataNot enough public salary data is available for this exact role. Before applying, prepare to ask about gross pay, benefits, contract length, probation period, transport and any allowances.
Can you qualify for this role?
- UnclearRelated work experienceThe text mentions experience, but the exact level should be confirmed at source.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in internship, entregador, clinical officerThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in ThikaThe vacancy is associated with this location.
- UnclearComfort with the Full Time contract termsConfirm hours, duration, probation and benefits at the original source.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- Role specificAcademic or professional certificates
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Clinical Officer evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Kenya Medical Research Institute (KEMRI) and the role in Thika.
- Add concrete examples related to internship, entregador, clinical officer, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from Advance Africa Kenya Jobs; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
- Plan to submit before the listed deadline: 2026-11-15.
Source and safety check
- Advance Africa Kenya Jobs
- Original source link available
- Application method is clear
- Deadline is available: 2026-11-15
- No major risk signal was detected in the captured text.
Never pay for interviews, shortlisting, medical checks, uniforms, or job placement. Confirm every application at the original source before sharing personal documents. Report suspicious listing.
Interview preparation
- What experience makes you a strong fit for this Clinical Officer role in internship, entregador?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Thika under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research Kenya Medical Research Institute (KEMRI) before the interview.
Ask what the first priorities will be in the role and how success will be measured.
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Original source description
Kenya Medical Research - KEMRI Clinical Officer - Thika Jobs
Kenya Medical Research - KEMRI Clinical Officer - Thika Jobs
Job Summary
Support implementation of clinical research activities through participant screening, enrolment, follow-up, clinical care and research data collection.
Provide clinical management services for cervical cancer prevention programmes and women living with HIV while ensuring compliance with research protocols and clinical standards.
Contribute to research documentation, participant care, capacity building and dissemination of scientific findings.
Key Responsibilities
- Clinical Care & Patient Management
- Provide clinical management services for cervical cancer prevention and care programmes.
- Deliver clinical services to women living with HIV in accordance with established treatment guidelines.
- Support participant assessment, diagnosis, treatment and follow-up activities.
- Ensure delivery of quality patient-centered clinical care within research settings.
- Research Participant Management
- Participate in screening, enrolment and follow-up of study participants.
- Support informed consent and participant engagement processes.
- Monitor participant progress throughout study implementation.
- Ensure adherence to study protocols and ethical research standards.
- Clinical Research Data Collection
- Collect and document clinical research data accurately and consistently.
- Maintain complete and accurate study records and source documentation.
- Support data quality assurance activities and protocol compliance.
- Assist in resolving clinical monitoring queries and data clarification requests.
- Counselling & Health Education
- Provide counselling support to participants as required.
- Educate study participants on HIV care, reproductive health and cervical cancer prevention.
- Participate in awareness campaigns, educational programmes and community engagement activities.
- Support participant retention and adherence initiatives.
- Research Documentation & Reporting
- Document study procedures, clinical findings and participant outcomes.
- Generate and draft clinical and study reports as required.
- Maintain accurate records in compliance with research and regulatory requirements.
- Support dissemination of research findings through reports, presentations and scientific activities.
- Training & Capacity Building
- Support team training and capacity-building initiatives.
- Participate in research seminars, workshops and study-specific learning programmes.
- Contribute to strengthening team competencies in protocol implementation and participant management.
- Share knowledge and best practices with study teams.
- General Responsibilities
- Participate in study meetings, seminars and operational reviews.
- Support implementation of research objectives and project deliverables.
- Perform any other duties assigned from time to time in support of
- research activities.
Qualifications
- Diploma in Clinical Medicine and Surgery or Community Health from a recognized institution.
- Valid registration and licensing with the Clinical Officers Council or relevant regulatory authority.
- Additional training in HIV care, reproductive health or clinical research will be an added advantage.
Experience
Minimum three (3) years of experience with direct involvement in patient care.
Demonstrated experience in HIV care and treatment is mandatory.
Experience providing reproductive health services, including cervical cancer screening and treatment, is mandatory.
Experience supporting clinical research activities and participant follow-up is an added advantage.
Exposure to public health, reproductive health or research environments is desirable.
Technical Skills
Clinical Assessment and Patient Management.
HIV Care and Treatment Services.
Cervical Cancer Screening and Prevention.
Reproductive Health Service Delivery.
Clinical Research Data Collection.
Research Documentation and Reporting.
Participant Screening and Enrolment.
Clinical Monitoring and Query Resolution.
Health Education and Counselling.
Medical Records Management.
Research Ethics and Protocol Compliance.
Community Health and Public Health Programmes.
Key Competencies
Teamwork and Collaboration.
Excellent Communication and Interpersonal Skills.
Strong Organizational Skills.
Attention to Detail and Accuracy.
Problem-Solving and Critical Thinking.
Ability to Work with Minimal Supervision.
Professional Ethics and Integrity.
Patient-Centered Approach.
Research and Documentation Skills.
Adaptability and Results Orientation.
Personal Attributes
Highly organized and dependable.
Compassionate and patient-focused.
Professional and ethical.
Self-motivated and proactive.
Strong commitment to quality healthcare and research excellence.
Able to work effectively in multidisciplinary teams.
How to apply
For more information and job application details, see;
Kenya Medical Research - KEMRI Clinical Officer - Thika Jobs
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