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Senior Biostatistician - Clinical Trials

Job in Rustenburg, 0202, South Africa
Listing for: Placements24
Full Time position
Listed on 2026-09-26
Job specializations:
  • Research/Development
    Clinical Research, Data Scientist, Research Scientist
  • Healthcare
    Clinical Research, Data Scientist
Job Description & How to Apply Below

About the Role

Our client is seeking a highly skilled Senior Biostatistician to play a critical role in their Clinical Trials unit based in Rustenburg . This position is integral to the design, analysis, and reporting of clinical research studies, ensuring the integrity and validity of data. You will collaborate closely with clinical researchers, data managers, and regulatory experts to provide statistical expertise throughout the trial lifecycle.

The ideal candidate possesses a strong quantitative background, extensive experience with statistical software, and a deep understanding of clinical trial methodologies. This role offers the chance to contribute to significant medical advancements and work within a supportive team dedicated to advancing patient care through rigorous scientific research in Rustenburg .

Key Responsibilities
  • Design clinical trial protocols, sample size calculations, and statistical analysis plans.
  • Perform complex statistical analyses of clinical trial data using SAS, R, or similar software.
  • Interpret study results and prepare statistical reports for regulatory submissions and publications.
  • Collaborate with investigators to ensure accurate data collection and study conduct.
  • Provide statistical consultation and support to research teams throughout the study duration.
  • Ensure adherence to Good Clinical Practice (GCP) and relevant regulatory guidelines.
Requirements
  • Master's or PhD degree in Biostatistics, Statistics, or a related quantitative field.
  • Minimum of 6 years of experience in biostatistics, with a significant focus on clinical trial analysis .
  • Proficiency in statistical programming languages such as SAS and R.
  • Strong understanding of statistical principles, study design, and regulatory requirements for clinical trials.
  • Excellent communication and interpersonal skills, with the ability to explain complex statistical concepts clearly.
  • Experience with data management and database querying is a plus.
Benefits
  • An excellent annual salary with annual reviews and potential bonuses.
  • Comprehensive health, dental, and vision insurance.
  • Retirement savings plan with company contributions.
  • Opportunities for continued professional development and advanced training.
  • A dynamic and collaborative work environment in Rustenburg .
  • The chance to contribute to life-changing medical research and development.
Position Requirements
10+ Years work experience
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