Kenya Medical Research Institute (KEMRI) is a State Corporation established through the Science and Technology (Amendment) Act of 1979, which has since been amended to Science, Technology and Innovation Act 2013. The 1979 Act established KEMRI as a National body responsible for carrying out health research in Kenya.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 Vacancy 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 Experience in Clinical trials will be an added advantage    Mandatory 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