Associate Director, Biostatistics (2)

CSL Ltd

Multiple Locations
**
Statistical strategy for clinical trials
Statistical methodologies for study design
Lead statistical strategy for planning and execution
** CSL Ltd is seeking an Associate Director of Biostatistics to lead statistical contributions in clinical development programs across multiple therapeutic areas. The ideal candidate will possess extensive experience in drug development, statistical methodologies, and regulatory submissions, while contributing to innovative study designs. **

Job Summary

  • The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program.
  • The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the program.
  • CSL Behring is a global biotherapeutics leader driven by our promise to save lives.

Matching Summary

Match Score: 75

** CSL Ltd is seeking an Associate Director of Biostatistics to lead statistical contributions in clinical development programs across multiple therapeutic areas. The ideal candidate will possess extensive experience in drug development, statistical methodologies, and regulatory submissions, while contributing to innovative study designs. **

Skills & Requirements

Must-have

  • Statistical strategy for clinical trials
  • Statistical methodologies for study design
  • Lead statistical strategy for planning and execution
  • Quantitative evaluation for clinical trials
  • Represent Biostatistics in regulatory interactions
  • Manage outsourcing operations or internal programmers

Nice-to-have

  • Innovative study design thought partnership
  • Track record of innovation preferred
  • Improvement initiatives within the department

Key Requirements

  • PhD with 8 years of experience or MS with 11 years of experience
  • Experience providing statistical leadership at compound/indication level
  • Leading roles in regulatory submissions
  • Familiarity with regulatory guidance and interactions
  • Good working knowledge of SAS and/or R

Work Rights

Not specified

Tailored Resume

Cover Letter