Oversee large and/or complicated product(s) or indication(s), which may require overseeing other Global Statistical Lead(s); Develop, lead, and serve as the primary point of contact for the statistical program strategy for a portfolio of products/programs; Influence across product life cycle through developing statistically compelling Evidence Generation Plans (EGP) in collaboration with Strategic Development 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
Requirements:
Doctorate in Statistics/Biostatistics and post-graduate statistical experience in the pharmaceutical industry or medical research including phase 3 drug development in metabolic diseases or cardiovascular outcome trials (CVOT); 10+ years of post-graduate statistical experience in the pharmaceutical industry or medical research; Statistical leadership/contribution to regulatory/reimbursement submissions; Life Cycle Drug Development Experience
Text:
Senior Director, Biostatistics Oversee large and/or complicated product(s) or indication(s), which may require overseeing other Global Statistical Lead(s); Develop, lead, and serve as the primary point of contact for the statistical program strategy for a portfolio of products/programs; Influence across product life cycle through developing statistically compelling Evidence Generation Plans (EGP) in collaboration with Strategic Development 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 Doctorate in Statistics/Biostatistics and post-graduate statistical experience in the pharmaceutical industry or medical research including phase 3 drug development in metabolic diseases or cardiovascular outcome trials (CVOT); 10+ years of post-graduate statistical experience in the pharmaceutical industry or medical research; Statistical leadership/contribution to regulatory/reimbursement submissions; Life Cycle Drug Development Experience
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