Study Doctor - Kisumu
2025-11-11T11:10:50+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 Doctor - Kisumu
Key Responsibilities:
- Collect, verify, and accurately document demographic, clinical, and lesion measurement data (including SOC ruler-based ACTG criteria and SS3D imaging).
- Implement and lead phased adoption of SS3D-supported lesion measurement, including provider training and transition from SOC-only measurement.
- Train and mentor clinical staff on ACTG protocols, SS3D use, and clinical research best practices to ensure protocol adherence and data integrity.
- Ensure participant safety, identify and manage adverse events, and coordinate with safety oversight bodies.
- Oversee day-to-day study operations, including initiation, execution, workflow optimization, direct observation, and time-motion studies.
- Manage data quality, including supervision of data collection and entry, accuracy checks, and quality control procedures.
- Coordinate communication across investigators, clinical teams, external partners, and stakeholders to support implementation and dissemination.
- Lead program evaluation activities, including usability, acceptability, feasibility assessments, and micro-costing.
- Support research funding and scientific output through grant writing, manuscript development, and reporting to funders and regulators, plus presenting findings.
- Oversee budget and resource management, including equipment procurement, expenditure tracking, and financial reporting.
Collect, verify, and accurately document demographic, clinical, and lesion measurement data (including SOC ruler-based ACTG criteria and SS3D imaging). Implement and lead phased adoption of SS3D-supported lesion measurement, including provider training and transition from SOC-only measurement. Train and mentor clinical staff on ACTG protocols, SS3D use, and clinical research best practices to ensure protocol adherence and data integrity. Ensure participant safety, identify and manage adverse events, and coordinate with safety oversight bodies. Oversee day-to-day study operations, including initiation, execution, workflow optimization, direct observation, and time-motion studies. Manage data quality, including supervision of data collection and entry, accuracy checks, and quality control procedures. Coordinate communication across investigators, clinical teams, external partners, and stakeholders to support implementation and dissemination. Lead program evaluation activities, including usability, acceptability, feasibility assessments, and micro-costing. Support research funding and scientific output through grant writing, manuscript development, and reporting to funders and regulators, plus presenting findings. Oversee budget and resource management, including equipment procurement, expenditure tracking, and financial reporting
Excellent listening and reading skills Mandatory Strong translation skills
1 MBChB or equivalent medical degree with a valid practising license Mandatory 2 Master’s degree in Public Health (MPH) or a relevant field (e.g., Epidemiology, Global Health, Clinical Research will be an added advantage Added Advantage 3 At least 2 years of demonstrated research experience in Clinical or implementation studies, preferably in HIV, oncology, or infectious diseases. Ability to write, review, and contribute to grant applications and secure research funding.
JOB-691319ba348f2
Vacancy title:
Study Doctor - 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 Doctor - Kisumu
Key Responsibilities:
- Collect, verify, and accurately document demographic, clinical, and lesion measurement data (including SOC ruler-based ACTG criteria and SS3D imaging).
- Implement and lead phased adoption of SS3D-supported lesion measurement, including provider training and transition from SOC-only measurement.
- Train and mentor clinical staff on ACTG protocols, SS3D use, and clinical research best practices to ensure protocol adherence and data integrity.
- Ensure participant safety, identify and manage adverse events, and coordinate with safety oversight bodies.
- Oversee day-to-day study operations, including initiation, execution, workflow optimization, direct observation, and time-motion studies.
- Manage data quality, including supervision of data collection and entry, accuracy checks, and quality control procedures.
- Coordinate communication across investigators, clinical teams, external partners, and stakeholders to support implementation and dissemination.
- Lead program evaluation activities, including usability, acceptability, feasibility assessments, and micro-costing.
- Support research funding and scientific output through grant writing, manuscript development, and reporting to funders and regulators, plus presenting findings.
- Oversee budget and resource management, including equipment procurement, expenditure tracking, and financial reporting.
Work Hours: 8
Experience in Months: 24
Level of Education: bachelor degree
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