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Research Assistant

Job in Durban, 4056, South Africa
Listing for: CAPRISA Careers
Full Time position
Listed on 2026-02-17
Job specializations:
  • Research/Development
    Research Scientist, Clinical Research
  • Healthcare
    Clinical Research
Job Description & How to Apply Below

Job Description

CAPRISA is an award-winning global research organisation located on the campus of the Nelson R Mandela School of Medicine in Durban, South Africa and undertakes research in HIV, TB and Covid at four clinical research sites in Kwa Zulu-Natal. CAPRISA’s goal is to undertake globally relevant and locally responsive research that contributes to understanding HIV Vaccines and Pathogenesis, Prevention and Epidemiology, the links between Tuberculosis and AIDS treatment and Covid-19.

CAPRISA is a UNAIDS Collaborating Centre for HIV Research and Policy and is recognised as a DSI-NRF Centre of Excellence in HIV Prevention and hosts the SAMRC HIV-TB Pathogenesis and Treatment Research Unit.

The successful incumbent will be based at the CAPRISA Headquarters in Durban.

Minimum Requirements
  • Master’s degree in Science, Medicine, Microbiology, Public Health or associated allied health professions.
  • Experience with manuscript preparation and science writing.
  • At least 1 science publication in a peer reviewed journal.
  • Knowledge of research ethics and regulatory processes.
  • Experience in supporting clinical trials.
  • Computer literate and advanced skills with MS Office and MS Project.
Added Advantages
  • Previous experience with regulatory submissions (SAHPRA and Ethics).
Competencies Duties & Responsibilities
  • Assist with developing and maintaining study Standard Operating Procedures
  • Manuscript preparation, medical writing, science presentations, and dissemination of research outputs.
  • Work in conjunction with trial study coordinators to obtain necessary documents for regulatory and ethics submissions.
  • Coordinate the collection and update of regulatory (SAHPRA/ETHICS/NHRD) documents (initial submissions, amendments, recertification, reports, ad-hoc correspondence, trial registry registration and updates) for an estimated 5 trials per annum.
  • Report writing in accordance with funder, sponsor and regulatory body requirements.
  • Provide research and administrative support as required.
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