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Medical Officer job at Infectious Diseases Research Collaboration
Posted by: great-volunteer
Posted date: 2025-Aug-06
Location: Uganda, Kampala
Medical Officer 2025-08-05T10:08:12+00:00 International Development Research Centre (IDRC) https://cdn.ugashare.com/jsjobsdata/data/employer/comp_1444/logo/Infectious%20Diseases%20Research%20Collaboration%20(%20IDRC%20).jpg https://idrc-crdi.ca/en FULL_TIME Uganda Kampala 00256 Uganda Professional Services Healthcare 2025-08-11T17:00:00+00:00 Uganda 8 Duties Brief - Participate in study patient evaluations and management, informed consent procedures, initial and follow up visits for all illnesses.
- Ensure accurate and proper completion of all study logs and case record forms.
- Participate in organization and filing of study case record forms, and generation of reports in collaboration with the Study Coordinators and Data Management team.
- Participate in Adverse Event reporting activities.
- Perform clinical examinations and basic laboratory evaluations
- Provide appropriate treatment for participants
- Provide guidance and support to junior staff such as clinical officers and nurses to develop and maintain their clinical practice
- Maintain confidentiality of records and research findings as appropriate
- Attend staff meetings
- Maintain effective interpersonal relationships with other staff and participants
Qualification Required - Study participants properly enrolled
- Study participants correctly evaluated and managed
- Case record forms completed correctly
- Laboratory results entered in the case record forms
- Departmental and staff meetings attended
JOB-6891d80c489d3 Vacancy title:
Medical Officer Jobs at:
International Development Research Centre (IDRC) Deadline of this Job:
Monday, August 11 2025 Duty Station:
Uganda | Kampala | Uganda Summary
Date Posted: Tuesday, August 5 2025, Base Salary: Not Disclosed JOB DETAILS: Duties Brief - Participate in study patient evaluations and management, informed consent procedures, initial and follow up visits for all illnesses.
- Ensure accurate and proper completion of all study logs and case record forms.
- Participate in organization and filing of study case record forms, and generation of reports in collaboration with the Study Coordinators and Data Management team.
- Participate in Adverse Event reporting activities.
- Perform clinical examinations and basic laboratory evaluations
- Provide appropriate treatment for participants
- Provide guidance and support to junior staff such as clinical officers and nurses to develop and maintain their clinical practice
- Maintain confidentiality of records and research findings as appropriate
- Attend staff meetings
- Maintain effective interpersonal relationships with other staff and participants
Qualification Required - Study participants properly enrolled
- Study participants correctly evaluated and managed
- Case record forms completed correctly
- Laboratory results entered in the case record forms
- Departmental and staff meetings attended
Work Hours: 8 Experience in Months: 12 Level of Education: bachelor degree Job application procedure Interested in applying for this job? Click here to submit your application now
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