Director Biostatistics - Hematology

Admincsl

Hybrid
10+ years clinical development experience
Phd or ms/ma in statistics
Regulatory submission leadership
The Director leads the full scope of statistical contribution to a clinical development program including life cycle management and regulatory submissions

Job Summary

  • The Director leads the full scope of statistical contribution to a clinical development program including life cycle management and regulatory submissions.
  • This role requires interpreting analysis results to ensure reporting accuracy in study reports, abstracts, and manuscripts while partnering with key stakeholders.
  • CSL Behring is a global biotherapeutics leader driven by a promise to save lives using innovative technologies across multiple therapeutic areas.

Matching Summary

The Director leads the full scope of statistical contribution to a clinical development program including life cycle management and regulatory submissions.

Skills & Requirements

Must-have

  • 10+ years clinical development experience
  • PhD or MS/MA in statistics
  • Regulatory submission leadership
  • CDISC standards knowledge
  • CRO management experience

Nice-to-have

  • Strong cross-functional collaboration skills
  • Experience with matrixed environments
  • Excellent communication abilities
  • Strategic analytical mindset
  • Ability to lead through influence

Key Requirements

  • 10+ years pharmaceutical industry experience
  • PhD or Master's degree in Statistics
  • Demonstrated leadership in regulatory submissions
  • Experience managing external partners like CROs

Work Rights

Not specified

Tailored Resume

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