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    Study Coordinator at - Nairobi, Kenya - Kenya Medical Research Institute - KEMRI

    Kenya Medical Research Institute - KEMRI
    Kenya Medical Research Institute - KEMRI Nairobi, Kenya

    Found in: beBee S2 KE - 4 days ago

    Kenya Medical Research Institute (KEMRI) background
    Full time
    Description

    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.

    Vacancy No. FN
    Duties and Responsibilities

    Develop an in-depth understanding of the study protocols, goals and logistics required to conduct research studies and implementation projects
    Develop clinical trial implementation plans in collaboration with investigators and relevant stakeholders
    Create Standard Operating Procedures (SOPs) that align with the study protocols
    Conduct training for research teams to always guarantee adherence to study SOPs at all times.
    Provide leadership in research studies through coordination and daily oversight of day-to-day implementation of study activities
    Coordinate the study team to ensure proper performance of study and project activities consistent with study protocols and SOPs
    Lead study recruitment with the support of study investigators and research team, including evaluating potential participants for inclusion in clinical trials in compliance to the study protocol

    Perform study visits and clinical assessments of study participants, document study procedures, and interpret laboratory results in collaboration with study PIs.

    Ensure proper documentation of all research participants in physical and electronic medical records
    Ensure participant safety through monitoring of clinical and laboratory adverse events
    Ensure timely reporting of adverse events and protocol deviations.
    Ensure participant privacy and confidentiality are maintained
    Compiling weekly clinical and study data and study reports in coordination with data manager
    Oversee and monitor study budget expenditure, including study resource utilization, cash flow and expenditures
    Maintain relationships with collaborating partners and the County Ministry of Health
    Coordinate communication with research staff and PI/Co-PIs/Co-Investigators
    Maintain regular communication with members of the research team
    Ensure regular and timely updates of clinical trial recruitment, follow-up, and data collection progress
    Work professionally and ethically with competence, accountability, and integrity
    Perform any other relevant duties as assigned by the study PIs

    Requirements


    Qualifications:
    Bachelor of Medicine and Surgery
    Be duly registered with the relevant professional body, holding valid practice license

    Other Desirable

    Qualifications:
    Knowledge in Cervical Cancer Screening and Prevention Clinical or research programs
    Attention to detail, critical thinking and problem-solving skills
    Interpersonal and communication skills
    Good communication skills
    Experience working in HIV care, either in a Clinical or Research setting
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