Jobs and Vacancies in Migori, Kenya



Kenya Medical Research Institute

Research Assistant - Migori

Migori, Kenya

ENGIE Energy Access (EEA)

Access Territory Lead - Migori

Migori, Kenya

Teachers Service Commission

Teacher (Post Primary Institutions) - Migori

Migori, Kenya

CIC Insurance Group

Sales Officers – Retail Life - Migori

Migori, Kenya


Stock Point Officer - Migori

Migori, Kenya

National Government Affirmative Action Fund

County Coordinator - Migori

Migori, Kenya

Cereals Growers Association (CGA)

Field Agribusiness Coordinator - Migori

Migori, Kenya

County Government of Migori

Board Member – County Trade Development Credit Scheme

Migori, Kenya

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Kenya Forest Service

Forest Ranger - Migori

Migori, Kenya

Closing: Apr 16, 2023

15 days remaining

Published: Mar 28, 2023 (4 days ago)

Job Requirements


Work experience:

Language skills:

Job Summary

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  • Diploma in Clinical Medicine and Surgery, Nursing or Medical Laboratory Science.
  • Phlebotomy certification from an accredited institution



  • Diploma in Clinical Medicine and Surgery, Nursing or Medical Laboratory Science.
  • Phlebotomy certification from an accredited institution

  • Work with study investigators to ensure study procedures are completed, specimens are collected, processed, and properly stored, and required data are collected
  • Locate and contact study participants

  • Administer informed consent to study participants and record the process appropriately

  • Respond to questions about the study posed by participants and other stake holders 

  • Develop in-depth understanding of the study’s goals and the logistics required to conduct the study 

  • Track/trace participants for their study visits within the prescribed visit windows to ensure good retention and safety monitoring

  • Complete CRFs

  • Administer questionnaires

  • Administer participant reimbursement.

  • Basic data management/data quality review in collaboration with the data science investigator

  • Collection of blood and urine samples from consented study participants

  • Sample handling, including packaging, chain of custody, preparation for transport to testing laboratories both locally and internationally. 

  • Travel on short notice to clinics, laboratory centers, and communities within the study regions

  • Coordination with other studies around documentation of participant consent, sample receipt, and sample collection kits

  • Report problems encountered to the study PI and consult appropriately 

  • Report adverse events as applicable and document all protocol deviations

  • Communicate with the Scientific Ethics Review Unit (SERU) and submit yearly reports, amendments, protocol deviations and renewals as required.

  • Maintain participant confidentiality at all times

  • Maintain good relationship with participants 

  • Maintain communication with team members in Kenya and the U.S., including communication via phone, email, Zoom, and other electronic means

  • Prepare for and attend regularly scheduled team meetings conducted virtually or in person

  • Due to working across time zones with the study team, and for participant recruitment, flexibility in working hours including evenings and occasionally weekends (for travel) is required.  

  • Perform any other relevant duties as assigned by the Principal Investigator and designated supervisors

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