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  • Entry Level

Registered Clinical Officer

KEMRI


Overview

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Vacancy Description
  • Entry Level
  • Nairobi
  • Applications have closed
About Company

Kenya Medical Research Institute (KEMRI)

19 Active Jobs (View all)
Industry: Healthcare

The Kenya Medical Research Institute (KEMRI) is a state corporation established through the Science and Technology (Amendment) Act of 1979, which has since been amended to Science, Technology and Innovation Act 2013 as the national body responsible for carrying out health research in Kenya.

Registered Clinical Officer – Nairobi

Key Responsibilities:

  • Provide high-quality clinical care to participants, including HIV testing, counselling.
  • Perform Phlebotomy
  • Conduct participant assessments, eligibility, diagnose medical conditions, and develop treatment plans in line with the study protocol.
  • Educate participants on Cholera prevention.
  • Collaborate with the research team to collect, document, and report clinical data accurately.
  • Ensure compliance with ethical, regulatory, and clinical guidelines in all activities.
  • Participate in training and capacity-building activities for clinic staff and community partners.
  • Informed Consent form administration
  • Administer respective Case Report Forms (CRFs)
  • Carrying out QA/QC of study CRFs, source docs, and resolve queries that may arise.
  • Develop and review of clinic related related SOPs

Vacancy Requirements:

  • Diploma in Clinical Medicine and Surgery
  • Valid Clinical officerโ€™s license to practice in Kenya.
  • Strong clinical and diagnostic skills.
  • Excellent communication and patient counselling skills.
  • Ability to work effectively in a multidisciplinary team.
  • Proficiency in electronic medical records (EMR) and data management systems.
  • Knowledge of ethical and regulatory requirements for clinical research.
  • Compassionate, patient-centred approach to care.
  • Strong organizational and time-management skills.
  • Commitment to advancing public health and HIV prevention.
  • Good Clinical Practice (GCP) and Human Subject Protection (HSP) certification with Strong knowledge of ICH guidelines
  • Maintain accurate and confidential participants records in compliance with site policies and regulations

Added Advantage

  • Experience in research settings or clinical trials will be an added advantage

Applications have closed
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