KEMRI Study Coordinator Jobs in Kenya

KEMRI Study Coordinator Jobs in Kenya



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

    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

    How to Apply

    For more information and job application details, see; KEMRI Study Coordinator Jobs in Kenya

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