CSL Behring is seeking an Associate Director of Biostatistics to lead the statistical contributions for clinical development programs. The ideal candidate will have extensive experience in drug development, statistical leadership, and regulatory submissions
Job Summary
Lead the full scope of statistical contribution to a clinical development program, providing statistical strategies for clinical trials and regulatory submissions.
Influence and contribute to clinical development plans, collaborate with cross-functional teams, and provide statistical thought partnership for innovative study designs.
Be responsible for interpreting analysis results, ensuring reporting accuracy, and managing outsourcing operations or internal statistical programmers.
Matching Summary
Match Score: 85
CSL Behring is seeking an Associate Director of Biostatistics to lead the statistical contributions for clinical development programs. The ideal candidate will have extensive experience in drug development, statistical leadership, and regulatory submissions.
Skills & Requirements
Must-have
Statistical strategy for clinical trials
Regulatory submission statistical deliverables
Advanced statistical methodologies
SAS and/or R proficiency
Biostatistics and Statistical Programming Operations
Nice-to-have
Innovative study design
Interactions with regulatory authorities
Management of outsourcing operations
Track record of innovation
Key Requirements
PhD with 8 years of experience or MS with 11 years of experience in drug development
Experience providing statistical leadership at compound/indication level