Associate Director, Biostatistics

CSL Behring

Phd or ms in biostatistics
8-11 years drug development experience
Statistical leadership at compound level
The Associate Director leads the full scope of statistical contribution to a clinical development program within a specific therapeutic area

Job Summary

  • The Associate Director leads the full scope of statistical contribution to a clinical development program within a specific therapeutic area.
  • This role involves providing statistical thought partnership for innovative study designs and Go-No Go criteria calculations.
  • CSL Behring is a global biotherapeutics leader driven by a promise to save lives through innovative therapies.

Matching Summary

The Associate Director leads the full scope of statistical contribution to a clinical development program within a specific therapeutic area.

Skills & Requirements

Must-have

  • PhD or MS in Biostatistics
  • 8-11 years drug development experience
  • Statistical leadership at compound level
  • Advanced statistical methodologies expertise
  • Regulatory submission experience
  • SAS and/or R programming knowledge

Nice-to-have

  • Experience with CRO management
  • Track record of innovation
  • CDISC and data standards familiarity
  • Strong interpersonal communication skills
  • Matrix environment collaboration

Key Requirements

  • PhD with 8 years experience OR MS with 11 years experience
  • Demonstrated statistical leadership in pre/early/full clinical development
  • Leading roles in regulatory submissions
  • Familiarity with regulatory guidance documents

Work Rights

Not specified

Tailored Resume

Cover Letter