Senior Principal Statistician

Roche/Genentech

South San Francisco, CA, USA
Statistical analysis plans
Sas and/or r proficiency
Clinical trial methodology expertise
This role ensures scientific rigor and regulatory compliance in clinical trials

Job Summary

  • This role ensures scientific rigor and regulatory compliance in clinical trials.
  • You will lead statistical design and strategy for molecule programs.
  • The position involves mentoring junior staff and contributing to scientific communication.

Matching Summary

This role ensures scientific rigor and regulatory compliance in clinical trials.

Skills & Requirements

Must-have

  • Statistical analysis plans
  • SAS and/or R proficiency
  • Clinical trial methodology expertise

Nice-to-have

  • Experience in obesity and diabetes
  • Mentoring within a matrix organization
  • Strategic mindset for portfolio decisions

Key Requirements

  • MSc or PhD in Statistics
  • Minimum 12 years of clinical development experience
  • Proven ability to lead statistical input

Work Rights

Not specified

Tailored Resume

Cover Letter