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.
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Participate in participant review and care, and all study procedures as guided by study protocols.
Perform pelvic exams, cervical cancer screening, contraceptive counselling administration, and removals
Perform phlebotomy on all study participants
Assess adherence to study products and take anthropometric measurements
Prepare weekly and monthly progress reports of study activities
Monitor adverse events and report them to the safety monitor as required.
Act as liaison between investigators, and participants.
Promote good clinical practice in the conduct of clinical studies and provide medical input at all stages of the project lifecycle
Perform any other job-related duties as may be requested or required
Vacancy Requirements:
Bcahelor’s Degree in Medicine and Surgery (MBChB Mandatory
A valid retention certificate from KMPDC Mandatory
Demonstrated competence in female reproductive health service delivery, including cervical cancer screening, counseling, and provision of various contraception methods Mandatory
Two years’ experience in a similar field. Mandatory
Experience in a research setting and having a Human Subject protection certificate will be an added advantage Added Advantage
Excellent interpersonal skills to deal effectively with clinicians, other study staff, participants, administrators, regulators, monitors, and sponsors. Mandatory
Familiarity with the Microsoft Office Suite. Mandatory
Excellent organizational skills to independently manage workflow. Mandatory
Ability to prioritize quickly and appropriately Mandatory