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Posted: 06 Mar 2017 09:02
Deadline: 10 Mar 2017
Category: Health Professionals
Location: Africa , Uganda , Kampala
Employment: Full-Time
Experience: From 3 year(s)
Education: Diploma
Salary: Negotiable
About Company: IDI is a Ugandan not-for-profit organisation whose Mission is to strengthen health systems in Africa, with a strong emphasis on infectious diseases, through research and capacity development. Established within Makerere University, the Institute began life in 2002 and currently provides care and treatment services to over 110,000 people living with HIV in urban and rural settings in Uganda (directly through our large clinic, and in partnership with government and non-government health facilities) which amounts to about 13% of the national effort. IDI also provides extensive prevention services (including medical male circumcision) and is a national referral centre for complicated cases of HIV.
Email: office@idi.co.ug
Phone: +256-31-2211422
Contact name: INFECTIOUS DISEASES INSTITUTE
File: Download
Requirements
•   Registered or enrolled Nurse’s training from a recognized institution
    •   Should be registered with the Uganda Nurses and Midwifes’ Council
    •   At least three years’ experience in Uganda Health Care
    •   Previous experience in research will be an added advantage
    •   Ability to travel within Uganda at short notice

Desirable skills & qualities:

    •   Excellent interpersonal and communications skills;
    •   Should be fluent in oral and written English;
    ■ Should be a highly motivated person and should be able to work under a high workload;
    •   Competent in the use of standard office software;
    •   Ability to work in a team but also work independently.
    •   Ability to speak local language
    •   Flexibility to work long hours which may occasionally extend beyond normal working hours in order to complete critical tasks.
Conditions
n/a
Responsibilities
•   Screen, recruit and consent study participants
    •   Assist prepare participants for study related clinical procedures
    •   Ensure that the study room and study equipment are clean, organized and maintained in good working order.
    •   Follow-up study patients, review patient files and labs results
    •   Perform any other clinical duties that may be reasonably necessary for implementing the study protocol
    •   Help with Clinical Research Form (CRF) filling, answering or adjudicating queries, and quality control of CRFs
    •   Filing and organization of study files
    •   Facilitating specimen collection, flow and result reporting.
    •   Providing pre, post, ongoing, supportive and any other form of counseling to participants in the study
    •   Attend all study team meetings
    •   Participate in and conduct all relevant Continuous Medical Education and trainings
    Ensure availability of relevant information about participants for follow up, support and care.
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