Clinical Officer

Hiring: NairobiCity Newsroom
Stato
Open
• Job Type Contract
• Qualification Diploma
• Experience 3 years
• Location Nairobi
• Job Field Medical / Healthcare
• 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
• 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
• Job Type Contract • Qualification Diploma • Experience 3 years • Location Nairobi • Job Field Medical / Healthcare • 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 • 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

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