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Baylor College of Medicine Children’s Foundation (Uganda)

Research Nurse

Kampala, Uganda

5 days remaining

Laterite

Research Analyst – Agriculture

Kampala, Uganda

4 days remaining

Makerere University Lung Institute

Research Fellow

Kampala, Uganda

1 day remaining

Lira University

Laboratory Assistant - Physiology Department

Lira, Uganda

3 days remaining

Lira University

Laboratory Assistant - Anatomy Department

Lira, Uganda

3 days remaining

UNICEF

Research & Evaluation Specialist

Kampala, Uganda

Closing today

National Agricultural Research Organization (NARO)

Research Officer - Aquaculture - Lira

Lira, Uganda

7 days remaining

National Agricultural Research Organization (NARO)

Senior Research Officer - Soil Scientist - Kawanda

Kawanda, Uganda

7 days remaining

National Agricultural Research Organization (NARO)

Research Officer - Animal Production - Arua

Arua, Uganda

7 days remaining

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Ministry of Internal Affairs (Uganda)

Senior Laboratory Technician

Kampala, Uganda

14 days remaining

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Fuzu

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Research Nurse

Closing: May 1, 2024

5 days remaining

Published: Apr 26, 2024 ( today)

Job Requirements

Education:

Work experience:

Language skills:

Job Summary

Contract Type:

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The Research Nurse will conduct clinical assessment of research participants. Recruit eligible study participants and provide nursing care and medical services to the study participants according to the study protocol. Develop required standard operating procedures. Submit event reports to regulatory bodies, IRB and the sponsor.

 


Requirements

  • Bachelor’s degree in Nursing from a recognized institution.
  • Training TB screening, prevention and treatment. HIV/AIDs treatment, prevention and research is an added advantage.
  • Two years of experience offering nursing care in a TB-HIV clinic, and research setting.


Responsibilities

The Research Nurse will conduct clinical assessment of research participants. Recruit eligible study participants and provide nursing care and medical services to the study participants according to the study protocol. Develop required standard operating procedures. Submit event reports to regulatory bodies, IRB and the sponsor.

 


Requirements

  • Bachelor’s degree in Nursing from a recognized institution.
  • Training TB screening, prevention and treatment. HIV/AIDs treatment, prevention and research is an added advantage.
  • Two years of experience offering nursing care in a TB-HIV clinic, and research setting.


  • Participate in the identification, screening and recruitment of eligible participants and ensure achievement of the target number of participants within the designated period, with close follow up as per study protocol to minimize participant loss-to-follow-up.
  • Give study information to eligible clients and obtain written informed consent from the participants and care takers.
  • Perform the required study Anthropometric measurements on all the study participants as per visit schedule in line with the study protocol and Good Clinical Practice (GCP) guidelines.
  • Provide initial and emergency treatment for any patients requiring admission and follow up these patients on the ward together with the study doctor according to the Uganda clinical guidelines, and prevailing national HIV/TB treatment guidelines. Provide clinical care to participants according to the Uganda clinical guidelines, national HIV and TB treatment guidelines.
  • Collect required samples for TB diagnosis such as induced sputum, naso-pharygneal aspirate, gastric lavage, stool and swabs.
  • Collect study data using provided tools such as electronic or paper-based Case Report Forms (CRFs) and source documents. File documents accordingly in line with the study protocol and Good Clinical Practice (GCP) guidelines.
  • Conduct quality control (QC) procedures on completed informed consent forms (ICFs) and CRFs from each station for accuracy and logical completion then document the Identified errors in the study error log. Make immediate alerts to the concerned study staff to rectify the errors, follow-up resolution of errors and forward the file to the filing clerk for data entry in a timely manner as per the Study Standard Operating Procedures (SOPs). Respond to data queries from routine QC/QA or site monitoring visit in line with the study protocol and Good Clinical Practice (GCP) guidelines.
  • Prepare and circulate minutes from meetings to key stakeholders. Prepare weekly study progress reports and any other reports as requested by the study coordinator and site investigator in line with the Study protocol.
  • Conduct follow-up home visits for clients receiving ART and TPT in the community, and supervise the community health workers, in line with the study protocol and GCP guidelines.
  • Participate in writing and review of study SOPs as per the need to clarify steps for critical procedures.


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