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MRC/UVRI Uganda Research Unit on AIDS
CLOSEDEntebbe, Uganda
MRC/UVRI Uganda Research Unit on AIDS
CLOSEDEntebbe, Uganda
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MRC/UVRI Uganda Research Unit on AIDS
CLOSEDEntebbe, Uganda
Closing: May 27, 2024
11 days remainingPublished: May 15, 2024 (2 days ago)
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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
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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