Principal Statistician

Hoffmann-La Roche Ltd

Mississauga, Canada
Base: $136,936.00 - $179,728.50 cad; bonus/equity:...
Not specified
Phd or msc in statistics or biostatistics
7+ years clinical trial statistics experience
Proficiency in sas and/or r programming
Roche is seeking a Principal Statistician to join their team in Mississauga, Canada. The role involves applying statistical expertise in the design and analysis of clinical trials, with a focus on driving innovation and ensuring regulatory compliance

Job Summary

  • This role is within Biostatistics, a core function providing strategic leadership and scientific rigor across Roche's Product Development Data Science and Analytics.
  • The Principal Statistician ensures the scientific rigor and regulatory compliance of studies by contributing to protocol development, authoring statistical analysis plans, and supporting result interpretation.
  • Roche offers a culture that encourages personal expression, open dialogue, and genuine connections where every voice matters to prevent, stop, and cure diseases.

Matching Summary

Match Score: 85

Roche is seeking a Principal Statistician to join their team in Mississauga, Canada. The role involves applying statistical expertise in the design and analysis of clinical trials, with a focus on driving innovation and ensuring regulatory compliance.

Salary

Base: $136,936.00 - $179,728.50 CAD; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • PhD or MSc in Statistics or Biostatistics
  • 7+ years clinical trial statistics experience
  • Proficiency in SAS and/or R programming
  • Deep familiarity with CDISC standards
  • Experience leading statistical contributions to regulatory submissions

Nice-to-have

  • Therapeutic experience in CVRM or Hematology/Oncology
  • Mentoring junior staff in matrix organizations
  • Strategic mindset for portfolio-level decisions
  • Ability to translate complex data for non-technical audiences
  • Experience with multiple phases of drug development

Key Requirements

  • PhD or MSc degree required
  • Minimum 7 years of clinical trial statistics experience
  • Advanced proficiency in SAS and/or R
  • Expertise in CDISC standards and regulatory requirements

Work Rights

Not specified

Tailored Resume

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