Research Study Interviewer - eThekwini

at  TB HIV Care

eThekwini, KwaZulu-Natal, South Africa -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate16 Aug, 2024Not Specified17 May, 20242 year(s) or aboveWorking Experience,EnglishNoNo
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Description:

JOB ADVERT SUMMARY

TB HIV Care (THC), in existence since 1929, is an internationally recognised non-profit organisation. We provide health care services throughout South Africa to both the general population and communities at increased risk for HIV and TB, including adolescent girls and young women, sex workers and people who use drugs. THC provides a stimulating work environment and the opportunity to work with leaders in the field of HIV and TB prevention and care. Our work culture is adapted to the constantly evolving South African health care environment and will suit solution-driven team players interested in opportunities for career development while working to connect people with care.

MINIMUM REQUIREMENTS

  • Grade 12 / matric
  • Office Administration qualification would be an advantage
  • Minimum 2 years working experience with demonstrated organisational knowledge and interview/survey experience
  • Familiarity with community-based research principles
  • Knowledge and experience in working / research with key populations, ideally with people who use drugs
  • Data capturing experience
  • Fluent in isiTswana, isiZulu, English or any other South African languages

Responsibilities:

PURPOSE OF THE POSITION:

The Research Study Interviewer is responsible for assessing eligibility for participation, obtaining informed consent and administering the survey questionnaire on a tablet/ computer. This will be part of a biobehavioural survey among female sex workers.

DUTIES AND RESPONSIBILITIES

  • Checking validity of study coupons
  • Registering the person’s fingerprint into the fingerprint management system
  • Screening the person for eligibility to participate in the survey
  • Providing brief information about the study to the potential participant and assessing willingness to participate (obtain informed consent)
  • Verify person’s fingerprint before conducting the survey questionnaire
  • Conduct a quantitative survey (± 35 minutes) with participants
  • Participate in site and related meetings around study implementation
  • Support data cleaning and checking processes
  • Support maintenance of appropriate files


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Hospital/Health Care

Pharma / Biotech / Healthcare / Medical / R&D

Health Care

Diploma

Proficient

1

eThekwini, KwaZulu-Natal, South Africa