KEMRI Research Administrator (Regulatory) Jobs in Mtwapa - Kenya

KEMRI Research Administrator (Regulatory) Jobs in Mtwapa - Kenya

Key Responsibilities:
  • Maintain studies’ compliance with applicable guidelines and regulations as well as all relevant local laws at all times,
  • Keep track of all study protocols at the various IRBs and the regulatory body with an aim of ensuring strict adherence to submission/reporting timelines,
  • Maintain documents as required by regulatory agency guidelines,
  • Organize, coordinate, and document all training undertaken in respect to the study and to file all the relevant training records,
  • Conduct periodic internal monitoring and audits of studies to ensure compliance with the protocol, SOPs, GCP and all the applicable regulations,
  • Tracking, documenting, and reporting adverse events,
  • Writing and reviewing of Standard Operating Procedures,
  • Developing of study source documents,
  • Any other duties assigned by the immediate supervisor.

    Vacancy Requirements:
  • Bachelor of Science Degree, Social Sciences or a health-related discipline
  • Training on Regulatory Affairs/Quality Assurance/Clinical trials will be an added advantage Added Advantage
  • Fluency in Kiswahili and English – both written and oral
  • Training in Good Clinical Practice (GCP) and other applicable regulations.

    How to Apply

    For more information and job application details, see; KEMRI Research Administrator (Regulatory) Jobs in Mtwapa - Kenya

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