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Clinician Job at The South African Medical Research Council (SAMRC)

Full Time
  • Full Time
  • Durban
  • PLEASE QUOTE THE REFERENCE NUMBER ( R285A ) IN ALL COMMUNICATIONS

Website The South African Medical Research Council (SAMRC)

The South African Medical Research Council is a para-statal medical research organisation in South Africa. The current president is professor Glenda Gray. The South African Medical Research Council was established in 1969. It is a member of the Innovative Vector Control Consortium

The South African Medical Research Council (SAMRC) strives to improve the nation’s health and quality of life by funding and conducting relevant and leading health research. It further aims to promote equity, career development and progression. The organisation prides itself on three core values: being pioneering, striving for excellence and working collaboratively.

The SAMRC retains the right not to make an appointment. Should no feedback be received within 30 days of the closing date, kindly consider your application as unsuccessful.

Vacancy Unit/Directorate Region Closing date

Clinician
Two – Year Contract

HIV Prevention Research Unit

Durban Westville Office
15 November 2019

The SAMRC’s HIV Prevention Research Unit (HPRU) requires the skills of a committed, motivated, suitably qualified and experienced clinician to work with the Principal Investigator and Clinical Site Research Leader in managing the clinical aspects of HIV prevention trials.

Responsibilities: Core Requirements:

  • Perform clinical activities related to the trial including clinical assessments, specimen collection, laboratory results review, oversight of the safety of study participants, determination of clinical eligibility, and administration of study product
  • Conduct clinical interviews and administer study questionnaires
  • Report, follow up, assess and manage adverse events
  • Complete all required study-related documentation according to the study protocol, Standard Operating Procedures (SOP) and Good Clinical Practice(GCP)requirements
  • Conduct regular quality control checks to ensure accuracy of clinical data collection and good quality data
  • Train new clinicians and nurses and capacitate the research team
  • Write reports as required
  • Contribute to unit publications
  • Undertake after hours and weekend work as required
  • Rotate across clinical research sites and provide back-up where and when required.
    • MBChB degree with at least 1-year post community service experience
    • HPCSA and MPS registration
    • Computer Literate

Advantageous

    • Proven clinical trial or research experience
    • Proven experience in ARV treatment
    • Trained in Advanced Cardiac Life Support (ACLS) or Advanced Life Support (ALS)
    • Trained in Good Clinical Practice
    • Sound communication and organizational skills within a multi-disciplinary team
    • A Code 8 manual drivers licence
    • Ability to multi-task and work under pressure.

A total cost-to-company remuneration package will be guided by reference of remuneration in the public sector and will be negotiated in accordance with experience. In accordance with the SAMRC’s Employment Equity Plan, preference will be given to suitably qualified candidates from the designated groups. For this reason, we require race, gender and disability status to be specified. Disabled persons are encouraged to apply.

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