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South African Medical Research Council jobs

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    • Review of research tools and documents.
    • Disability and GBV research experience of 6 months or more.
    • The South African Medical Research Council, Gender and…
    • Review of research tools and documents.
    • Disability and GBV research experience of 6 months or more.
    • The South African Medical Research Council, Gender and…
    • Present research findings at local and international conferences.
    • Experience presenting research findings at local and international scientific conferences.
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    • Previous experience of stakeholder liaison in a scientific research environment.
    • Support the design and implementation of health policy analysis and/or health…
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    • Experience within the public sector, research environment, or higher education sector will be advantageous.
    • Reporting to the Executive Director: Human Resources…

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Job Post Details

Senior Research Technician(S): Data Collector - job post

South African Medical Research Council
4.2 out of 5 stars
Durban, KwaZulu-Natal
Part-time
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Job details

Job type

  • Part-time

Location

Durban, KwaZulu-Natal

Full job description

The South African Medical Research Council, Gender and Health Research Unit (GHRU) requires suitably qualified Senior Research Technician (S): Data Collector to support our disability and SRHR-related research and training projects.


Responsibilities:

  • Assisting in implementing study protocols and SOPs
  • Translation and Transcribing
  • Supporting research implementation (e.g.
  • Conducting of interviews and focus group discussions
  • Quality control of interviews and group discussions
  • Review of research tools and documents
  • Providing disability accommodation and support
  • Recruit participants
  • Conduct informed consent and enrollment of participants
  • Keep data management log and other monitoring tools up to date
  • Prepare and print all relevant documents for the fieldwork
  • Contact and engage with stakeholders' participants to prepare meetings and events
  • Support meeting preparations to ensure everything is set for the meeting
  • Prepare reimbursement and arrange travel for participants
  • Filling and record keeping of source
  • File informed consent and other
  • Recruitment forms as per SOPs
  • Labeling and filing source documents

Duration:

6 Months


Core Requirements:

  • Grade 12/NQF level 4
  • Good Clinical Practice certification
  • Disability and GBV research experience of 6 months or more
  • Experience working with people with disabilities
  • Experience in translating and transcribing
  • Experience in qualitative data collection
  • 6 months -1 years’ experience in qualitative methods for data collection

Advantageous:

Any experience greater than that which is stated above


Closing Date:

14 July 2026

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