Director Biostatistics

Role Summary

Director Biostatistics

Responsibilities

• Develop, lead, and serve as the primary point of contact for the statistical program strategy for a portfolio of complex programs
• Influence across product life cycle through developing statistically compelling Evidence Generation Plans (EGP) in collaboration with Strategic Development Director, Director, Statistical Innovation, EDL, GDL, GMAL, and Regional Medical Leads
• Partner with evidence-related, cross-functional stakeholders to ensure the highest statistical standards and integrity and provide program level statistical support

Qualifications

• Doctorate in Statistics/Biostatistics and post-graduate statistical experience in the pharmaceutical industry or medical research and at least 8 years of post-graduate statistical experience
• Or Master‚Äôs degree in Statistics/Biostatistics or related subject with high statistical content and at least 10 years of post-graduate statistical experience
• Preferred: Doctorate in Statistics/Biostatistics with 8 years of post-graduate statistical experience in Oncology/Hematology therapy area of at least 4 years
• Or Master‚Äôs degree and 12 years of Biostatistics experience in the pharmaceutical industry or medical research in Oncology/Hematology therapy area of at least 4 years

Skills

• Statistical methodologies, trial design, data analysis, and medical/clinical understanding for product
• Collaboration with cross-functional teams to drive innovative designs, standards, quality, and evidence synthesis
• Strategic input for regulatory interactions and evidence generation planning

Education

• PhD or Master‚Äôs with extensive experience in biostatistics or statistics as detailed in Qualifications