Attachment - Nakuru (147 Slots) at Kenya Pipeline Company (KPC) Limited

Key Responsibilities: Morning and afternoon charting of the Investigational Product (IP) room temperatures Shipment of IPs as requested. Receiving and storage of the IPs at the IP room Ensure proper tracking of all the IPs. Respond to any queries raised regarding the IPs Completing all the necessary documentation Liaison with site study staff in relation to the IPs Daily, weekly and monthly stock taking of the IPs Dispensing IPs to the Study participants Attend regular departmental meetings and CMEs Give instructions to the participants on the IPs usage. Perform other duties that may be given by the supervisor Vacancy Requirements: Diploma in Pharmacy from a recognized institution Mandatory Experience in Research and in Clinical Trials will be an added advantage Added Advantage Good communication skills and responsive to emails and phone calls Mandatory Computer literate Mandatory Detail oriented Mandatory Registered and Licenses by Pharmacy and Poisons Board Mandatory

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 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