Director Biostatistics

CSL SEQIRUS

Hybrid (3 days in office, occasional travel)
10+ years clinical development experience
Phd or ms/ma in statistics
Regulatory submission expertise
CSL Seqirus is seeking a Director of Biostatistics who will lead statistical contributions to clinical development programs, ensuring statistical excellence in study design, data analysis, and regulatory submissions. The ideal candidate will have over 10 years of experience in the pharmaceutical or biotechnology industry, with strong leadership and collaboration skills

Job Summary

  • The role leads the full scope of statistical contribution to a clinical development program including life cycle management.
  • Candidates must demonstrate the ability to interact with health authorities such as the FDA, EMA, and PMDA.
  • This is a hybrid position requiring three in-office days per week with occasional travel to scientific conventions.

Matching Summary

Match Score: 85

CSL Seqirus is seeking a Director of Biostatistics who will lead statistical contributions to clinical development programs, ensuring statistical excellence in study design, data analysis, and regulatory submissions. The ideal candidate will have over 10 years of experience in the pharmaceutical or biotechnology industry, with strong leadership and collaboration skills.

Skills & Requirements

Must-have

  • 10+ years clinical development experience
  • PhD or MS/MA in statistics
  • Regulatory submission expertise
  • CDISC standards knowledge
  • Cross-functional team collaboration

Nice-to-have

  • Experience managing external CROs
  • Strong communication skills
  • Matrixed environment leadership
  • Strategic analytical mindset

Key Requirements

  • 10+ years pharmaceutical industry experience
  • PhD or MS/MA degree in statistics
  • Proven leadership in regulatory submissions

Work Rights

Not specified

Tailored Resume

Cover Letter