Senior Statistical Analyst (Hybrid)

Role Summary

The Senior Statistical Analyst supports research and development of new pharmaceutical products by analyzing and reporting clinical trial data and leading statistical programming activities for clinical studies of lower complexity. The role interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations. This is a hybrid on-site role; candidates must be local to Lake County, IL; Florham Park, NJ; San Francisco, CA or Irvine, CA.

Responsibilities

• Leads the statistical programming activities for projects with lower complexity.
• Leads the statistical programming activities for studies.
• Develop SAS programs for the creation of ADaM data sets following CDISC standards.
• Develop SAS programs for the creation of Tables, Listings and Figures.
• Validation of ADaM data sets, Tables, Listings and Figures.
• Create specifications for the structure of ADaM data sets for individual studies and integrated data.
• Create documentation for regulatory filings including reviewers guides and data definition documents.
• Leads the development of standard SAS Macros and participates in the development of standard operating procedures.
• Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.

Qualifications

• MS in Statistics, Computer Science or a related field with 6+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 8+ years of relevant experience.
• In-depth understanding of SAS programming concepts and techniques related to drug development.
• Fundamental understanding of CDISC Standards.
• Fundamental understanding of the drug development process, including experience with regulatory filings.
• Ability to communicate clearly both oral and written.
• Ability to accurately estimate effort required for study related programming activities.