Data Collector: Wits Health Consortium

Data Collector

Location: Johannesburg

Closing Date: 13 February 2026

Responsibilities and Duties

  • Support study activities, including conducting site initiation visits, performing  assessments, preparing study sites, and coordinating with key stakeholders.
  • Manage project logistics and provide day-to-day support to the project.
  • Ensure that the study protocol is followed and that procedures are consistently and accurately maintained.
  • Conduct study recruitment and informed consent process following protocol and ethical requirements.
  • Complete electronic survey forms on laptops/mobile tablets and securely transfer data to an appropriate server.
  • Conduct patient record review and data collection from paper files and electronic data sources
  • Contribute to data collection activities by independently performing data collection activities, which may include:
    • Survey interviews, or
    • Qualitative interviewing (in-depth interviews, semi-structured interviews, focus group discussions).
  • Manage stakeholder engagements and relationships.
  • Consistently implement data standard operating procedures to ensure the confidentiality and security of all data collected at all project sites.
  • Ensure neat and accurate filing and tracking of data forms

Requirements

  • At least 1 year of research work experience enrolling and interviewing research participants
    in a medical environment.
  • Matric certificate required, diploma and/or degree are desirable.
  • Fluency in English and at least one other local language preferred (preferably IsiZulu, SePedi, shiVenda and Xitsonga). Strong verbal and written English communication skills.
  • Strong working knowledge of health facilities and data systems.
  • Previous experience in conducting interviews and qualitative and/or quantitative data
    collection in research settings.
  • Experience in performing clinical assessments on study participants.
  • Aptitude/willingness to share health information and to provide support and guidance to
    study participants.
  • Excellent computer literacy, especially in Microsoft Excel and Word. Experience with mobile data collection systems will be advantageous.
  • Ability to work effectively as a team player with a diverse group of people and senior staff, including researchers and senior researchers.
  • Ability to work within the setting of busy clinics in a friendly and non-disruptive manner.
  • Good Clinical Practice and ethics training and a valid certificate is preferred.
  • Excellent organizational skills, high attention to detail, and ability to take initiative.
  • Ability to travel, including overnight trips.
  • Code 8 Driver’s License, at least 12 months of driving experience and willingness to drive.

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