Statistical Analyst, Statistical Programmer

Summary

Join AbbVie as a Statistical Analyst and play a key role in the research and development of new pharmaceutical products. This integral position involves analyzing and reporting clinical trial data, both independently and with supervision. You will collaborate with statisticians, data scientists, and development operations teams. Responsibilities include developing SAS programs, validating data sets and reports, and creating documentation for regulatory filings. The ideal candidate possesses a strong background in statistics or computer science and proven SAS programming skills within the pharmaceutical industry.

Requirements

• MS in Statistics, Computer Science or a related field with 3+ years of relevant experience
• OR BS in Statistics, Computer Science or a related field with 5+ years of relevant experience
• Demonstrated practical understanding of SAS programming concepts and techniques related to drug development
• Basic understanding of CDISC Standards
• Basic understanding of the drug development process
• Ability to communicate clearly both oral and written

Responsibilities

• Lead the statistical programming activities for routine 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
• Validate ADaM data sets
• Validate 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 for SAS Macros, as well as, presenting information on existing Macros
• Participate in the development of standard SAS Macros

Benefits

• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k)
• Short-term incentive programs