The Director leads the full scope of statistical contribution to a clinical development program including life cycle management and regulatory interactions
Job Summary
The Director leads the full scope of statistical contribution to a clinical development program including life cycle management and regulatory interactions.
This role requires defining statistical strategies and ensuring appropriate methodologies are applied to study designs and data analysis for robust results.
CSL Behring is a global biotherapeutics leader driven by a promise to save lives through innovative therapies in immunology and hematology.
Matching Summary
The Director leads the full scope of statistical contribution to a clinical development program including life cycle management and regulatory interactions.
Skills & Requirements
Must-have
10+ years clinical development experience
PhD or MS/MA in statistics
Regulatory submission expertise
CDISC standards knowledge
CRO management experience
Nice-to-have
Strong communication skills
Matrixed environment leadership
Strategic analytical mindset
Cross-functional collaboration
Key Requirements
10+ years pharmaceutical industry experience
PhD or Master's degree in Statistics
Demonstrated leadership in statistical contributions