Associate Director, Biostatistics (4)

CSL Behring

Multiple Locations
**
Statistical strategy for clinical trials
Regulatory submission statistical deliverables
Advanced statistical methodologies
** CSL Behring is seeking an Associate Director of Biostatistics to lead statistical contributions for clinical development programs. The ideal candidate will have significant experience in drug development and regulatory submissions, along with strong leadership and communication skills. **

Job Summary

  • Lead the full scope of statistical contribution to a clinical development program, defining statistical strategies for trials and regulatory submissions.
  • Provide statistical thought partnership for innovative study design, clinical development plans, and quantitative evaluations.
  • Represent Biostatistics in interactions with regulatory authorities and ensure accuracy in study reports and regulatory documents.

Matching Summary

Match Score: 75

** CSL Behring is seeking an Associate Director of Biostatistics to lead statistical contributions for clinical development programs. The ideal candidate will have significant experience in drug development and regulatory submissions, along with strong leadership and communication skills. **

Skills & Requirements

Must-have

  • Statistical strategy for clinical trials
  • Regulatory submission statistical deliverables
  • Advanced statistical methodologies
  • SAS and/or R proficiency
  • Biostatistics leadership

Nice-to-have

  • Track record of innovation
  • Interactions with regulatory authorities
  • Managing CROs or internal deliveries
  • Improvement initiatives

Key Requirements

  • PhD with 8 years or MS with 11 years of experience in drug development
  • Experience providing statistical leadership at compound/indication level
  • Leading roles in regulatory submissions

Work Rights

Not specified

Tailored Resume

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