Associate Director/Director, Biostatistics | Northbrook, Illinois, United States | Astellas Pharma US, Inc.

Position:	Associate Director/Director, Biostatistics
Institution:	Astellas Pharma US, Inc.
Location:	Northbrook, Illinois, United States
Duties:	Accountable for multiple projects, providing leadership and advising project teams and statistical leads by challenging statistical design, analysis and decision-making issues; Provides expert opinions, advises staff on available statistical methodologies, performs/supervises modeling and simulations, and leverages external experts to provide input to clinical development issues; Provides oversight on statistical matters for meetings with regulatory authorities, key opinion leaders and similar experts; Provides statistical leadership and consultancy to address authority requests, publication, presentation and other external sharing of results; Reviews key project level documents and advises other statisticians on design and methodologies
Requirements:	PhD or M.S in Biostatistics, Statistics or related scientific field; 2+ years of demonstrated experience in working on global clinical studies and projects or global process and system initiatives

Text:	Associate Director/Director, Biostatistics Accountable for multiple projects, providing leadership and advising project teams and statistical leads by challenging statistical design, analysis and decision-making issues; Provides expert opinions, advises staff on available statistical methodologies, performs/supervises modeling and simulations, and leverages external experts to provide input to clinical development issues; Provides oversight on statistical matters for meetings with regulatory authorities, key opinion leaders and similar experts; Provides statistical leadership and consultancy to address authority requests, publication, presentation and other external sharing of results; Reviews key project level documents and advises other statisticians on design and methodologies PhD or M.S in Biostatistics, Statistics or related scientific field; 2+ years of demonstrated experience in working on global clinical studies and projects or global process and system initiatives