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Study Nurse

Closing: Jun 16, 2024

1 day remaining

Published: Jun 6, 2024 (9 days ago)

Job Requirements

Education:

Work experience:

Language skills:

Job Summary

Contract Type:

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Essential Requirements:

  • Diploma in Nursing   
  • Registered with the Nursing Council of Kenya.   
  • At least two (2) years Clinical research experience   
  • Demonstrated competence in female reproductive health service delivery, including cervical cancer screening, counselling, and provision of various contraception methods   
  • Knowledge of HIV prevention and treatment services   
  • Good Clinical Practice training/Human Subjects Protection training in mental Health/Psychiatry Nursing, is an added advantage    Added Advantage
  • Commitment to integrity and high-quality performance   
  • Good interpersonal skills and ability to work in a team   
  • Keen and attentive to detail   
  • Ability to follow instructions and procedures   
  • Articulate in both verbal and written communication in English and Swahili.   
  • Counselling skills   
  • Computer literacy


Responsibilities

Essential Requirements:

  • Diploma in Nursing   
  • Registered with the Nursing Council of Kenya.   
  • At least two (2) years Clinical research experience   
  • Demonstrated competence in female reproductive health service delivery, including cervical cancer screening, counselling, and provision of various contraception methods   
  • Knowledge of HIV prevention and treatment services   
  • Good Clinical Practice training/Human Subjects Protection training in mental Health/Psychiatry Nursing, is an added advantage    Added Advantage
  • Commitment to integrity and high-quality performance   
  • Good interpersonal skills and ability to work in a team   
  • Keen and attentive to detail   
  • Ability to follow instructions and procedures   
  • Articulate in both verbal and written communication in English and Swahili.   
  • Counselling skills   
  • Computer literacy


  • Prescreening and screening of participants
  • Register and consent study participants and assist with eligibility determination, screening, and enrolment of study participants.
  • Informed Consent administration per study protocol and collection of participant medical, surgical and reproductive history.
  • Support in health talks to participants at the clinic and mobilization sources.
  • Respond to questions about the study posed by participants and the community in consultation with the study doctor.
  • Maintain up-to-date participant visit notes
  • Administer Case Report Forms (CRFs), accurate recording of data on CRFs, and perform self-
  • Perform phlebotomy on all study participants
  • Assess adherence to study products and take anthropometric measurements
  • Closely work with other staff members to ensure the success of the study


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