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  • Posted: Jun 6, 2024
    Deadline: Jun 25, 2024
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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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    Study Physician/Study Coordinator

    Key Responsibilities:

    • Oversee all clinic and other study personnel performing study specific tasks and procedures.
    • Monitors adverse events and reports them to the safety monitor as required.
    • Act as liaison between investigators, participants and staff.
    • Ensure preparedness of staff and site for study implementation.
    • Provide training, mentorship to clinical team in all aspects of trial conduct and project orientation to ensure compliance with protocols and guidance documents
    • Promote good clinical practice in the conduct of clinical studies and provide medical input at all stages of the project lifecycle
    • Participate in participant review and care, and in all study procedures as guided by study protocols.
    • Oversee regulatory submissions and approvals to local ethical review committees and liaise with other project managers to ensure timely submissions to international institutional review boards.
    • Maintain all study records including but not limited to, regulatory binders, study specific source documentation and other materials as required.
    • Coordinates and facilitates monitoring and auditing visits, notifies appropriate institutional officials audits, responses to any findings and implements approved recommendations.
    • May perform other job-related duties as requested or required

    Vacancy Requirements:

    • Degree in Medicine and Surgery (MBChB)
    • At least 3-year work experience as a medical officer
    • Experience and competence in providing HIV care clinical care services
    • Previous management and leadership experience    Added Advantage
    • Experience providing reproductive health services.    Added Advantage
    • Knowledge of clinical trial ethics and Good Clinical Trial Practice    Added Advantage
    • Must have valid retention certificate from KMPDC
    • Excellent interpersonal skills.
    • Familiarity with the Microsoft Office Suite.
    • Excellent organizational skills to independently manage work flow.
    • Ability to prioritize quickly and appropriately
    • Ability to multi-task.
    • Meticulous attention to detail

    Check how your CV aligns with this job

    Method of Application

    Interested and qualified? Go to Kenya Medical Research - KEMRI on erecruitment.kemri.go.ke to apply

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