Mar 1, KEMRI Study Coordinator Jobs in Kenya

mar-1,-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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