Study Nurse - Kisumu
2025-11-11T11:11:06+00:00
Kenya Medical Research Institute ( KEMRI )
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https://www.kemri.go.ke/
FULL_TIME
Kisumu
Kisumu
00100
Kenya
Healthcare
Science & Engineering, Research, Healthcare
2025-11-18T17:00:00+00:00
Kenya
8
Job Tite/Designation
Study Nurse - Kisumu
Key Responsibilities:
- Provide study information, address participant questions, and support retention through scheduled clinical assessments and follow-up coordination.
- Assist with lesion measurements, skin biopsy procedures, and safe handling of biological samples per protocol and SOPs.
- Label, package, transport, and track samples, coordinating closely with KEMRI and Washington University laboratories for receipt, storage, and shipment documentation.
- Record participant data in CRFs and study databases accurately and promptly, ensuring data quality through collaboration with the Data Manager.
- Maintain secure, organized clinical and research records in compliance with protocol requirements.
- Support qualitative research activities, including planning, recruitment, transcription, and secure data handling.
- Participate in study operations with the clinical and data management team, providing weekly progress updates on recruitment, follow-up, and data entry.
- Assist in resource management including supply procurement, inventory control, and basic financial/budget tracking.
- Prepare and submit regulatory documents to relevant ethics and oversight bodies, including amendments, safety reports, and deviations.
Provide study information, address participant questions, and support retention through scheduled clinical assessments and follow-up coordination. Assist with lesion measurements, skin biopsy procedures, and safe handling of biological samples per protocol and SOPs. Label, package, transport, and track samples, coordinating closely with KEMRI and Washington University laboratories for receipt, storage, and shipment documentation. Record participant data in CRFs and study databases accurately and promptly, ensuring data quality through collaboration with the Data Manager. Maintain secure, organized clinical and research records in compliance with protocol requirements. Support qualitative research activities, including planning, recruitment, transcription, and secure data handling. Participate in study operations with the clinical and data management team, providing weekly progress updates on recruitment, follow-up, and data entry. Assist in resource management including supply procurement, inventory control, and basic financial/budget tracking. Prepare and submit regulatory documents to relevant ethics and oversight bodies, including amendments, safety reports, and deviations.
research or clinical trials
1 Bachelor’s Degree in Nursing Mandatory 2 Master’s in public health, Nursing and related courses is an added advantage Added Advantage 3 Minimum of 2–3 years of research experience in research settings or clinical trials is highly desirable
JOB-691319ca04b98
Vacancy title:
Study Nurse - Kisumu
[Type: FULL_TIME, Industry: Healthcare, Category: Science & Engineering, Research, Healthcare ]
Jobs at:
Kenya Medical Research Institute ( KEMRI )
Deadline of this Job:
Tuesday, November 18 2025
Duty Station:
Kisumu | Kisumu | Kenya
Summary
Date Posted: Tuesday, November 11 2025, Base Salary: Not Disclosed
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JOB DETAILS:
Job Tite/Designation
Study Nurse - Kisumu
Key Responsibilities:
- Provide study information, address participant questions, and support retention through scheduled clinical assessments and follow-up coordination.
- Assist with lesion measurements, skin biopsy procedures, and safe handling of biological samples per protocol and SOPs.
- Label, package, transport, and track samples, coordinating closely with KEMRI and Washington University laboratories for receipt, storage, and shipment documentation.
- Record participant data in CRFs and study databases accurately and promptly, ensuring data quality through collaboration with the Data Manager.
- Maintain secure, organized clinical and research records in compliance with protocol requirements.
- Support qualitative research activities, including planning, recruitment, transcription, and secure data handling.
- Participate in study operations with the clinical and data management team, providing weekly progress updates on recruitment, follow-up, and data entry.
- Assist in resource management including supply procurement, inventory control, and basic financial/budget tracking.
- Prepare and submit regulatory documents to relevant ethics and oversight bodies, including amendments, safety reports, and deviations.
Work Hours: 8
Experience in Months: 24
Level of Education: bachelor degree
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