Associate Director, Biostatistics

csl.co.th

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Phd or ms in biostatistics
8-11 years drug development experience
Statistical leadership at compound level
** The Associate Director of Biostatistics at CSL Behring is responsible for leading statistical contributions to clinical development programs, including strategy formulation for clinical trials and regulatory submissions. The ideal candidate should possess advanced statistical expertise, extensive experience in drug development, and strong leadership skills within a collaborative team environment. **

Job Summary

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

Matching Summary

Match Score: 75

** The Associate Director of Biostatistics at CSL Behring is responsible for leading statistical contributions to clinical development programs, including strategy formulation for clinical trials and regulatory submissions. The ideal candidate should possess advanced statistical expertise, extensive experience in drug development, and strong leadership skills within a collaborative team environment. **

Skills & Requirements

Must-have

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

Nice-to-have

  • Innovative study design capabilities
  • Experience with CRO management
  • CDISC and data standards expertise
  • Strong communication skills
  • Matrix environment collaboration

Key Requirements

  • PhD with 8 years experience OR MS with 11 years
  • Leadership in pre/early/full clinical development strategy
  • Solid experience in advanced statistical methodologies
  • Leading roles in regulatory submissions
  • Interactions with major regulatory authorities preferred

Work Rights

Not specified

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