Tms & Data Analytics Analyst — Power Bi For Logistics

Anonymous; Gauteng; On-site; ZAR 900,000 - 1,500,000; Full time

Job summary

Anonymous in Sandton, Gauteng seeks a Biostatistician to lead statistical design of clinical trials and rigorous analysis of complex data to support drug development.

You will interpret study results and contribute to regulatory submissions, working within a data-driven clinical research team in a leading pharmaceutical organization.

Qualifications

• Master's or PhD required in Biostatistics, Statistics, or related field.
• Minimum of 5 years of pharmaceutical/biotech Biostatistics experience.
• Proficiency in SAS or R; SAS preferred.

Responsibilities

• Design clinical trial SAPs and specify study endpoints.
• Perform statistical analyses of trial data using SAS or R, including data exploration and hypothesis testing.
• Interpret results and contribute to CSRs and regulatory submission documents.
• Provide statistical expertise to development teams, statisticians and project managers.
• Ensure quality and integrity of analyses through validation and documentation.
• Contribute to development and implementation of innovative statistical methodologies for trial design and analysis.

Skills

Statistical design

Data interpretation

Regulatory submissions

Education

Master's or Ph.D. in Biostatistics/Statistics

Tools

SAS

R

Job description

Biostatistician - Sandton

Our client is seeking a highly analytical Biostatistician to join their data-driven clinical research team in Sandton . In this role, you will be responsible for the statistical design of clinical trials and the rigorous analysis of complex clinical data to support drug development. Your expertise will be essential in interpreting study results and contributing to regulatory submissions. This is a key position within a leading pharmaceutical organization, offering the chance to apply advanced statistical methodologies to impactful research within the bustling Gauteng financial hub.

Key Responsibilities

• Design clinical trial statistical analysis plans (SAPs) and specify study endpoints.
• Perform statistical analyses of clinical trial data using SAS or R, including data exploration, hypothesis testing, and modeling.
• Interpret statistical results and collaborate with medical writers to prepare clinical study reports (CSRs) and regulatory submission documents.
• Provide statistical expertise and consultation to clinical development teams, study statisticians, and project managers.
• Ensure the quality and integrity of statistical analyses through rigorous validation and documentation processes.
• Contribute to the development and implementation of innovative statistical methodologies for clinical trial design and analysis.

Requirements

• Master's or Ph.D. in Biostatistics, Statistics, or a related quantitative field.
• Minimum of 5 years of experience as a Biostatistician in the pharmaceutical or biotechnology industry.
• Proficiency in statistical software such as SAS (preferred) or R, including experience with advanced