The role leads the full scope of statistical contribution to a clinical development program within a specific therapeutic area
Job Summary
The role leads the full scope of statistical contribution to a clinical development program within a specific therapeutic area.
Candidates must provide 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
The role leads the full scope of statistical contribution to a clinical development program within a specific therapeutic area.
Skills & Requirements
Must-have
PhD or MS in Biostatistics
8-11 years drug development experience
Statistical leadership at compound level
Advanced statistical methodologies expertise
Regulatory submission experience
Nice-to-have
Innovative study design capabilities
Experience with major regulatory authorities
CRO management experience
Track record of innovation
Strong interpersonal communication skills
Key Requirements
PhD with 8 years experience OR MS with 11 years
Solid experience in pre/early/full clinical development strategy
Leading roles in regulatory submissions
Expertise in CDISC and statistical programming standards