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Research Administrator (Regulatory) - Mtwapa

Closing: Jul 23, 2024

11 days remaining

Published: Jul 4, 2024 (9 days ago)

Job Requirements

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Job Summary

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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.

To apply for this post you must be a registered user. Log into your account then go to Vacancies, view the post and click on the button: "Apply for this job".

  • Candidates must supply an email and telephone contact that will be used when offering interviews. Only shortlisted candidates will be contacted. Shortlisted candidates shall be required to produce ORIGINALS of their National Identity Card, academic and professional certificates, original transcripts and testimonials, detailed curriculum vitae and valid clearance certificate (certificate of good conduct) during the interviews.


Responsibilities

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.

To apply for this post you must be a registered user. Log into your account then go to Vacancies, view the post and click on the button: "Apply for this job".

  • Candidates must supply an email and telephone contact that will be used when offering interviews. Only shortlisted candidates will be contacted. Shortlisted candidates shall be required to produce ORIGINALS of their National Identity Card, academic and professional certificates, original transcripts and testimonials, detailed curriculum vitae and valid clearance certificate (certificate of good conduct) during the interviews.


  • 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.


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