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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Provide high-quality clinical care to participants, including HIV testing, counselling, and prescription of oral PrEP.
Conduct participants assessments, diagnose medical conditions, and develop treatment plans in line with the study protocol protocols.
Support the implementation and monitoring of clinical procedures related to the study protocol.
Educate participants on HIV prevention, PrEP adherence, and sexual health.
Collaborate with the research team to collect, document, and report clinical data accurately.
Ensure compliance with ethical, regulatory, and clinical guidelines in all activities.
Safety assessment and reporting
Perform Phlebotomy, and contraceptive method administration and Sexual Reproductive Health Assessments
Administer respective Case Report Forms (CRFs)
Carrying out QA/QC of study CRFs, source docs, and resolve queries that may arise.
Develop and review of study related related SOPs
Participate in training and capacity-building activities for clinic staff and community partners.
Maintain accurate and confidential participants records in compliance with Site’s policies and regulations.
Vacancy Requirements:
Bachelor of Medicine and Bachelor of Surgery (MBChB) or equivalent medical degree Mandatory
Valid practicing license Mandatory
Minimum of 2–3 years of clinical experience, preferably in HIV care, sexual health, or infectious diseases. Mandatory
Experience in research settings or clinical trials is highly desirable. Mandatory
Familiarity with Contraceptive method administration, PrEP ,PrEP guidelines and HIV prevention strategies/interventions is a plus. Mandatory
Strong clinical and diagnostic skills. Mandatory
Excellent communication and patient counselling skills. Mandatory
Ability to work effectively in a multidisciplinary team Mandatory
Proficiency in electronic medical records (EMR) and data management systems. Mandatory
Knowledge of ethical and regulatory requirements for clinical research. Mandatory
Compassionate, patient-cantered approach to care. Mandatory
Strong organizational and time-management skills. Mandatory
Commitment to advancing public health and HIV prevention Mandatory
Ability to oversee/supervise a team Mandatory
Good Clinical Practice (GCP) and Human Subject Protection (HSP) certification with Strong knowledge of ICH guidelines, FDA, PPB, and other global regulatory frameworks Mandatory
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