Statistician

Roche Holding AG

Not specified
Msc or phd in statistics or biostatistics
Minimum 2 years clinical trial statistics experience
Proficiency in sas and/or r programming
Roche Holding AG is seeking a Statistician within their Biostatistics team, responsible for applying statistical expertise to clinical trials. The position requires a strong educational background in statistics or biostatistics, relevant experience in clinical trial statistics, and proficiency in statistical software

Job Summary

  • The Statistician is a key member of the cross-functional study team responsible for applying statistical expertise to the design, conduct, analysis, and interpretation of individual clinical trials.
  • This role ensures scientific rigor and regulatory compliance by contributing to protocol development, authoring statistical analysis plans, and supporting the interpretation of results for regulatory submissions.
  • Roche fosters a culture that encourages personal expression, open dialogue, and genuine connections where every voice matters in the mission to prevent, stop, and cure diseases.

Matching Summary

Match Score: 85

Roche Holding AG is seeking a Statistician within their Biostatistics team, responsible for applying statistical expertise to clinical trials. The position requires a strong educational background in statistics or biostatistics, relevant experience in clinical trial statistics, and proficiency in statistical software.

Skills & Requirements

Must-have

  • MSc or PhD in Statistics or Biostatistics
  • Minimum 2 years clinical trial statistics experience
  • Proficiency in SAS and/or R programming
  • Familiarity with ICH guidelines and GCP regulations
  • Knowledge of CDISC standards for data

Nice-to-have

  • Experience translating complex concepts for non-technical audiences
  • Strategic mindset for portfolio-level decisions
  • Ability to work effectively in cross-functional global teams
  • Experience across multiple phases of drug development

Key Requirements

  • MSc or PhD in Statistics, Biostatistics, or related quantitative field
  • Minimum 2 years relevant experience in clinical trial statistics
  • Strong understanding of FDA and EMA regulatory requirements

Work Rights

Not specified

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