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  • Posted: Jul 15, 2025
    Deadline: Aug 4, 2025
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  • 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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    Nurse - 2 Posts

    Key Responsibilities:

    • Provide high-quality nursing care to participants,
    • Conduct participant’s assessments, monitor vital signs, and assist in the diagnosis and treatment of medical conditions.
    • Obtaining informed consent and enrolment of participants into study.
    • Explaining study procedures to eligible participants
    • Obtains medical history and performs physical examination
    • Offers individual, group and family counseling to participants and patients
    • Confirms eligibility for all study participants
    • Conducts protocol specific tests and procedures
    • Providing project management team with regular feedback on participant recruitment.
    • Provide HIV counseling, testing and lab results interpretation
    • Verify quality of data by comparing abstracted data to source documents
    • Responds to participant’s calls
    • Administer the oral cholera vaccine and perform phlebotomy.
    • Retention activities-follow up of participants in need of close monitoring and review together with visit reminders via phone calls
    • Record any adverse events and notify the lead clinician of the same as per protocol
    • Performs other duties as may be assigned
    • Collaborate with the research team to collect, document, and report clinical data accurately.
    • Administer Case Report Forms and perform quality checks
    • Ensure compliance with ethical, regulatory, and clinical guidelines in all activities.
    • Participate in training and capacity-building activities for clinic staff and community partners.

    Vacancy Requirements:

    • Diploma in Nursing    Mandatory
    • Excellent written and verbal communication skills in both English and Kiswahili.    Mandatory
    • Training in GCP and Human subjects will be an added advantage.    Added Advantage
    • Experience with current methods of epidemiology surveillance; having worked in a multidisciplinary, multi-site project will be an added advantage    Added Advantage
    • Registered with the Nursing Council of Kenya    Mandatory
    • Team player    Mandatory
    • Excellent Communication and people skills    Mandatory
    • Highly organized    Mandatory
    • Ability to work without supervision    Mandatory

    go to method of application »

    Registered Clinical Officer

    Key Responsibilities:

    • Provide high-quality clinical care to participants, including HIV testing, counselling.
    • Perform Phlebotomy
    • Conduct participant assessments, eligibility, diagnose medical conditions, and develop treatment plans in line with the study protocol.
    • Educate participants on Cholera prevention.
    • Collaborate with the research team to collect, document, and report clinical data accurately.
    • Ensure compliance with ethical, regulatory, and clinical guidelines in all activities.
    • Participate in training and capacity-building activities for clinic staff and community partners.
    • Informed Consent form administration
    • 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 clinic related related SOPs

    Vacancy Requirements:

    • Diploma in Clinical Medicine and Surgery    Mandatory
    • Valid Clinical officer’s license to practice in Kenya.    Mandatory
    • Experience in research settings or clinical trials will be an added advantage    Added Advantage
    • 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-centred approach to care.    Mandatory
    • Strong organizational and time-management skills.    Mandatory
    • Commitment to advancing public health and HIV prevention.    Mandatory
    • Good Clinical Practice (GCP) and Human Subject Protection (HSP) certification with Strong knowledge of ICH guidelines    Mandatory
    • Maintain accurate and confidential participants records in compliance with site policies and regulations    Mandatory

    go to method of application »

    Research Assistant

    Key Responsibilities:

    • Organizing and supervising the implementation of all laboratory activities
    • Work with Research Administrator to ensure adherence to study deliverables time points and support the submission of periodic reports on project status
    • Developing and designing local training and capacity building of project staff in collaboration with the study manager
    • Development of Lab SoPs and training staff on the same.
    • Liaising with relevant county and sub-county health management teams, MOH departmental heads, opinion leaders and other stakeholders
    • Drafting, editing and preparing correspondence, reports and other project related materials
    • Supporting quality assurance/quality control processes for the study data collection procedures
    • Translate study tools and documents from English into local language as necessary.

    Vacancy Requirements:

    • Bachelor’s Degree in Biomedical Science or a health related discipline; Public Health, Nursing, Clinical Medicine, Community Health from a recognized institution    Mandatory
    • Training in Good Clinical Practice    Mandatory
    • Molecular Biology and Bioinformatics skills will be an added advantage    Added Advantage

    Method of Application

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