Clinical Officer
AI summary
KEMRI is hiring a Clinical Officer in Nairobi to manage patient care within clinical research trials. The role involves screening and enrolling study participants, conducting examinations, administering investigational products, and reporting on clinic activities. A Clinical Medicine Diploma, board registration, and at least three years of clinical experience are required.
- Employer is Kenya Medical Research Institute (KEMRI)
- Deadline is 06/10/2026
- Requires Diploma in Clinical Medicine & Surgery
- At least 3 years clinical or clinical research experience required
- Registration certificate and valid practicing license mandatory
- Experience in clinical trials is an added advantage
- Salary listed as open
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Source salary availableThe source lists Open. Confirm the final pay, benefits, contract terms and allowances directly with the employer before accepting an offer.
Can you qualify for this role?
- Required3+ years of relevant experienceThe job post includes a minimum experience signal.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in entregador, Clinical Officer, HealthcareThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in Not specifiedThe vacancy is associated with this location.
- UnclearComfort with the Contract 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
- VerifyLicence, permit or professional registration
- 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 and the role in Not specified.
- Add concrete examples related to entregador, Clinical Officer, Healthcare, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from Corporate Staffing Kenya; 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: 2026-10-06.
Source and safety check
- Corporate Staffing Kenya
- Original source link available
- Application method is clear
- Deadline is available: 2026-10-06
- 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 entregador, Clinical Officer?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Not specified 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 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
Job Title: Clinical Officer
Date Posted: 30/09/2026
Job Type: Full Time
Job Level: Middle
Employer: Kenya Medical Research Institute
Industry: Medical
Salary: Open
Location: Nairobi
Country: Kenya
Deadline: 06/10/2026
Medical Jobs, KEMRI Jobs. Clinical Officer manages patient care in research trials, requires a Clinical Medicine Diploma, board registration, and 3+ years clinical experience.
Key Responsibilities
- Screen, consent, and enroll study participants who meet eligibility criteria, ensuring full adherence to ethical standards and study protocols.
- Conduct baseline and follow-up physical examinations, and provide routine clinical care, including daily ward rounds for study participants.
- Safely administer the investigational product in line with the approved study protocol.
- Diagnose and manage incidental illnesses, while monitoring, documenting, and reporting any side effects related to the investigational product.
- Make informed clinical decisions on participant admission, continued care, or referral as guided by the study protocol.
- Review study questionnaires to ensure data accuracy, completeness, and consistency before entry.
- Prepare and present weekly and monthly reports on clinic activities, including enrollment status, exclusions, reasons for exclusion, and follow-up plans.
- Maintain accurate tracking of participant visits, including initial and follow-up appointments, to monitor progress and ensure proper clinic attendance.
- Collect, label, and track biological specimens, ensuring proper handling, timely delivery to the laboratory, and support oversight of laboratory processes.
- Conduct verbal autopsies for community deaths occurring outside the facility to ensure complete and accurate reporting.
- Manage stock and inventory to maintain adequate and well-organized supplies at the study site.
- Perform any additional duties assigned
Requirements
- Diploma in Clinical Medicine & Surgery Mandatory
- At least three (3) years working experience in clinical research or in a busy clinic setting Mandatory
- Registration certificate and valid practicing license from the relevant professional body Mandatory
- Experience in Clinical trials will be an added advantage Added Advantage
- Proficient in computer applications, including Microsoft Word, Excel, PowerPoint, Zoom, and email communication tools. Mandatory
- Strong ability to manage multiple tasks efficiently and prioritize work in a fast-paced environment. Mandatory
- Demonstrated capacity to work effectively as part of a multidisciplinary team, contributing positively to shared goals. Mandatory