Associate Director, Statistical Programming

July 24

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Immunovant

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Dedicated to enabling normal lives for people with autoimmune diseases

Biotechnology Research

51 - 200

Description

• Responsible for performing programming and statistical analyses necessary to analyze clinical trial results • Validates/crosschecks the relevance and accuracy of statistical programs and resulting TLGs developed by external CROs • Participates in the development and maintenance of SAS macro library and safety database

Requirements

• Master’s degree in a quantitative sciences discipline (e.g., Statistics, Mathematics, Computer Science) and a minimum of 10 years in statistics or statistical programming in a biotech/pharmaceutical or CRO environment • Bachelor’s degree in a quantitative sciences discipline (e.g., Statistics, Mathematics, Computer Science) and a minimum of 12 years in statistics or statistical programming in a biotech/pharmaceutical or CRO environment • Excellent SAS programming skills (e.g., Base SAS, SAS/Stat, SAS/Graph, SAS macros, ODS) and a good understanding of database systems • Experience in lead programming activities involving CDISC SDTM, ADaM, eSub • Applied knowledge of clinical data analysis and reporting process as it relates to drug development • Excellent interpersonal and communication skills • Good organizational skills with the ability to adapt and adjust to changing priorities • Experience with CRO oversight • Regulatory submission experiences. Have lead programming activities involving CDISC SDTM, ADaM, eSub

Benefits

• Equity, sign-on bonuses, and other forms of compensation may be provided as part of a total compensation package • Full range of medical, dental, vision, 401k and other benefits • Unlimited paid time off • Parental leave