Research Nurse – Masiphumelele Job at Desmond Tutu Health Foundation

Job role overview

  • Date posted

    May 15, 2026

  • Closing date

    May 28, 2026

  • Hiring location

    Limpopo

  • Qualification

    National Certificate

  • Experience

    2 - 3 years

Description

Requirements

  • A Diploma or Degree in Nursing (General or Community)
  • Active registration as a Professional Nurse with the South African Nursing Council (SANC)
  • At least 2-3 years of working experience as a Nurse
  • Knowledge of HIV and TB
  • Knowledge of study protocols / regulations
  • Excellent computer literacy with sound knowledge of email, Excel, Word processing and Internet
  • Excellent ability to build interpersonal relationships
  • Strong planning and organising ability
  • Strong verbal, written and interpersonal communication skills
  • Ability to work well under pressure and to maintain effectiveness during changing conditions
  • Ability to work harmoniously with people of diverse backgrounds and sexuality
  • Client-focused
  • Ability to work independently and as part of a team
  • Ability to foster a collaborative relationship with participants
  • Must be detail orientated
  • Strong organizational skills, including time management and multi-tasking skills
  • Administration skills
  • Maintaining strict client confidentiality
  • Preference will be given to candidates residing in or near Masiphumelele, Fish Hoek, or Muizenberg due to operational requirements
  • Valid driver’s license (Code B)

Advantageous:

  • 1-2 year’s nursing experience in primary healthcare clinic
  • Fluency in IsiXhosa 
  • Current valid GCP certification

Responsibilities:

  • Manage the scheduled screening, consenting, enrolment and follow-up of participants including home visits, if required
  • Participate in research studies including recruitment and enrolment, day-to-day management of study procedures, capturing data queries from monitoring
  • Working across several studies
  • Conduct all work in compliance with internationally recognized ethical and good clinical practice standards
  • Assist study coordinator in clinic functions and administrative tasks. Administrative tasks include QC of files, filing of results, calling of patients etc
  • Refer all relevant queries to study coordinator
  • Conducting phlebotomy and specimen processing
  • Perform all clinical observations and procedures as required by research protocols and on request from study coordinator (e.g. draw blood, swabs, vital signs)
  • Identify potential volunteers from database and discussion groups
  • Perform participant interviews and counselling as per protocol requirements
  • Transcribe research data into case report forms as needed
  • Inform study coordinator of daily clinic progress
  • Manage samples (or liaise with the Laboratory Technician) as per protocol requirements
  • Maintain and record cold chain temperatures
  • Assist laboratory staff with testing procedures and quality control when required
  • Ensure that all samples are collected by the respective laboratories before close of business and leaving site
  • Assist in transporting participants between clinics and research site
  • Ensure all clinical areas and equipment are maintained in good order
  • Check medical waste boxes and bins and arrange collection thereof
  • Provide participants with advice and guidance on basic medical conditions
  • Oversee participant visits and ensure participants move through all study procedures efficiently
  • Participate in conference calls, meetings and training when required
  • Assist in inventory, ordering and equipment management
  • Manage all participant reimbursements

How to Apply

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