Biostatistician

Roche UK

Not specified; not specified; not specified
Msc or phd in statistics or biostatistics
Clinical trial statistics experience
Proficiency in sas and/or r programming
The role involves independently leading statistical input into clinical trial design to ensure scientific rigor and regulatory compliance

Job Summary

  • The role involves independently leading statistical input into clinical trial design to ensure scientific rigor and regulatory compliance.
  • Biostatistics at Roche leverages data to drive scientifically rigorous programmatic decisions across the company's development portfolio.
  • Roche fosters a culture of personal expression and open dialogue where every voice matters in the mission to prevent, stop, and cure diseases.

Matching Summary

The role involves independently leading statistical input into clinical trial design to ensure scientific rigor and regulatory compliance.

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • MSc or PhD in Statistics or Biostatistics
  • Clinical trial statistics experience
  • Proficiency in SAS and/or R programming
  • Knowledge of CDISC standards
  • Experience with protocol development

Nice-to-have

  • Cross-functional global study team experience
  • Mentoring less experienced statisticians
  • Strategic mindset for portfolio decisions
  • Ability to translate complex concepts
  • Early and late stage drug development experience

Key Requirements

  • Confirmed experience in clinical trial statistics
  • Solid understanding of regulatory expectations
  • Demonstrated experience across different phases
  • Capacity for independent thinking and decision making

Work Rights

Not specified

Tailored Resume

Cover Letter