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Clinical Officer

Closing: Jun 16, 2024

2 days remaining

Published: Jun 6, 2024 (8 days ago)

Job Requirements

Education:

Work experience:

Language skills:

Job Summary

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Essential Requirements:

  • Diploma in Clinical Medicine   
  • Valid practicing license.   
  • At least two (2) years Clinical research experience   
  • Demonstrated competence in female reproductive health service delivery, including cervical cancer screening, counseling, 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    Added Advantage
  • Computer literacy


Responsibilities

Essential Requirements:

  • Diploma in Clinical Medicine   
  • Valid practicing license.   
  • At least two (2) years Clinical research experience   
  • Demonstrated competence in female reproductive health service delivery, including cervical cancer screening, counseling, 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    Added Advantage
  • Computer literacy


  • Performing Clinical Assessments.
  • Collecting specimens.
  • Conducting interviews, administering Case report forms, and form completion
  • Offer support counseling to study participants.
  • Conducting the informed consent process.
  • Diagnose and provide STI and treatment for other ailments to participants.
  • Make requisitions for the required clinical supplies.
  • Monitor Adverse events and write reports to IRB or any other regulatory body as required
  • Develop and implement Standard Operating Procedures as per protocol
  • Perform any other duties as assigned by immediate supervisor.
  • Safety communication with the medical director, study safety monitor, and Principal Investigator


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