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Statistician

Job in Durban, 4056, South Africa
Listing for: Afrique Connection Consultancy
Full Time position
Listed on 2026-01-22
Job specializations:
  • Research/Development
    Research Scientist, Clinical Research, Data Scientist
  • Healthcare
    Clinical Research, Data Scientist
Job Description & How to Apply Below

Our client seeks to appoint a Statistician who will be responsible for providing statistical support and methodological advice for clinical studies. The incumbent will also be responsible for statistical analysis of studies, writing up of results as well as providing monthly reports on studies. The successful incumbent will join the team based in Durban.

Minimum Requirements
  • Masters or Honours degree in Biostatistics, Statistics or a related quantitative discipline (with undergraduate in a related quantitative discipline)
  • 4 years of research and statistical analysis experience
  • SAS, R, STATA or another statistical analysis programme essential
  • Basic knowledge of clinical research and epidemiology
  • High level of computer literacy in MS office (Word, Advanced Excel and Outlook)
  • Experience analysing clinical trial data or longitudinal data would be advantageous
Personal Qualities and Competencies
  • Exceptional organizational and problem-solving skills
  • Analytical ability with high attention to detail
  • Able to work under pressure in a changing environment
  • Ability to work independently and fit in well within a multi-disciplinary team
  • Ability to communicate statistical concepts to non-statisticians
  • Managing time and work/deadline driven
  • Excellent written, verbal communication skills and interpersonal skills
Key Responsibilities
  • Provide statistical advice for the design of clinical trials and different types of observational studies and contribute to protocols and grant applications
  • The ability to undertake projects in Biostatistical methodology and applied Biostatistical research; or being a co-investigator or study statistician in health-related project
  • Determine and undertake appropriate analysis of clinical trials, observational studies and de-identified routine health records data and record statistical analysis code in a reproducible format.
  • Write-up study design, sample size, statistical analysis plans and study analysis results
  • Prepare routine and adhoc study reports and contribute to presentations and publications
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