RESEARCH PROFESSIONAL NURSE: Division of Medical Microbiology Department of Pathology

  • Contract
  • Cape Town, Western Cape, Rondebosch, 7700 View on Map
  • University of Cape Town posted 4 weeks ago
  • Posted : Aug 26, 2021 -Accepting applications
  • Salary: R222,629.00 - R415,041.00 / Annual
  • View(s) 128

Job Detail

  • Offered Salary The annual cost of employment is dependent on experience within the Payclass 8 range (R222 629 to R415 041)
  • Qualifications Bachelor Degree
  • Industry Research, science & technology
  • Reference E21802
  • Centre UCT
  • Where to submit application
    To apply, please e-mail the below documents in a single pdf file to Reyhana Solomon at [email protected] . UCT Application Form (download at http://forms.uct.ac.za/hr201.doc). Cover letter, and Curriculum Vitae (CV) Please ensure the title and reference number are indicated in the subject line.
  • Notes
    An application which does not comply with the above requirements will be regarded as incomplete. Only shortlisted candidates will be contacted. The starting date is negotiable but preferably as soon as possible.

Job Description

The Division of Medical Microbiology invites applications from suitably qualified candidates for a 12-month contract position as a Research Professional Nurse. We are looking for an individual who wants to be part of a dynamic research group to assist with the recruitment and care of the clinical trial participants, collection of specimens and data. This post is based at Nolungile Clinic and at the Department of Medical Microbiology within the Faculty of Health Sciences at the University of Cape Town. Requirements: NQF 7 qualification in Nursing Science or equivalent. 3 years of relevant experience. Computer literacy. Good communication skills (verbal and written, both English and Xhosa). SANC registration. Good Clinical Practice Certificate The following will be advantageous:. Code B/08 driver’s license. Standard Bank Cashless system Responsibilities:. Participant assessment, recruitment and ensuring informed consent. Clinical Assessment. Clinic operations as relevant to the study. Data collection and management. Communication and collaboration. General adhoc duties and research administration

Required skills

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