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Entry and Basic-level Medical, health jobs in Kampala, Uganda
5
jobs
Walimu
CLOSEDClinical Nurse
Kampala, Uganda
Infectious Disease Institute
CLOSEDSmc Clinical Officer
Kampala, Uganda
Medical Teams International
CLOSEDSonographer
Kampala, Uganda
Medical Teams International
CLOSEDPsychiatric Clinical Officer
Kampala, Uganda
Medical Teams International
CLOSEDTheatre Assistant
Kampala, Uganda
Makerere University Joint AIDS Program
CLOSEDMedical Officer (ROM PROJECT)
Kampala, Uganda
Makerere University Joint AIDS Program
CLOSEDLocum ART Counselor
Kampala, Uganda
Infectious Disease Institute
CLOSEDDistrict Care & Treat Officer
Kampala, Uganda
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EMERGENCY Life Support for Civilian War Victims (EMERGENCY)
CLOSEDHospital Pharmacist
Kampala, Uganda
Closing: Apr 24, 2024
This position has expiredPublished: Apr 18, 2024 (24 days ago)
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Job Summary
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Requirements
• Completion of nurses’ training from a recognized institution (minimum of a certificate in nursing).
• Must hold a valid practicing license.
• Minimum of 1 year’s work experience in a clinical research setting
• Up-to-date registration with the Uganda Nurses and Midwives Council.
• Working use of Microsoft word, excel and the internet is essential
• Excellent Communication skills with patients, clinicians and with other members of the team.
• Ability to be a good team player.
• Knowledge of good nursing procedures and practices.
• Human Research Subject Protection and GCP training is an added advantage
Responsibilities
Requirements
• Completion of nurses’ training from a recognized institution (minimum of a certificate in nursing).
• Must hold a valid practicing license.
• Minimum of 1 year’s work experience in a clinical research setting
• Up-to-date registration with the Uganda Nurses and Midwives Council.
• Working use of Microsoft word, excel and the internet is essential
• Excellent Communication skills with patients, clinicians and with other members of the team.
• Ability to be a good team player.
• Knowledge of good nursing procedures and practices.
• Human Research Subject Protection and GCP training is an added advantage
• Contribute to identification of eligible patients at the health facility.
• Provide required study information to potential participants during the informed consent process and at different time points during their participation.
• Administer study questionnaires to participants recruited into the study, as per the protocol.
• Ensure that study samples from participants recruited into the study are drawn and handled in an appropriate and timely manner (as per the study protocol).
• Ensure that all collected data (including laboratory data) are recorded in the electronic database (i.e., REDCap) in an accurate, complete and timely manner, as per the guidance project coordinator and/or PI.
• Participate in regular quality control (QC) activities, including daily data QC, sample collection and storage QC, among others.
• Identify patient problems, including adverse events, documenting pertinent information and assisting patients in formulating plans for addressing problem areas.
• Contribute to development of Standard Operating Procedure (SOP) documents.
• Adhere to and remain knowledgeable about the SOPs, protocol and other key project documents.
• Maintain research documents according to GCP requirements.
• Participate in producing harmonized quality project reports.
• Treat each participant and colleague with dignity, respect and professionalism.
• Participate in study team meetings as scheduled by the site team leader, project coordinator and the PI.
• Taking minutes in collaborative meetings.
• Complete any additional tasks assigned by the site team leader, project coordinator and/or PI.
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