AbbVie is hiring a Statistical Programmer to support the research and development of new pharmaceutical products. The role focuses on analyzing and reporting clinical trial data, preparing regulatory documentation, and creating and validating analysis datasets and reports.
Create documentation for regulatory filings including reviewers guides and data definition documents
Participate in the development of standard SAS Macros
Consolidate heterogeneous data sources (e.g. clinical study databases, external databases, real-world data) to prepare analysis-ready data sets within a defined quality control process supporting a particular study
Perform exploratory data analyses and visualizations in interaction with the clinical pharmacologist or pharmacometrician
Produce dynamic and static data visualizations to communicate quantitative analyses
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
Validation of Tables, Listings and Figures
Create specifications for the structure of ADaM data sets for individual studies
Qualification
Required
MS in Statistics, Computer Science or a related field with 0+ years of relevant experience
BS in Statistics, Computer Science or a related field with 2+ years of relevant experience
Demonstrated practical understanding of SAS programming or NONMEM concepts and techniques
Ability to communicate clearly both oral and written
Preferred
Benefit
Paid time off (vacation, holidays, sick) for eligible employees
Medical, dental, and vision insurance for eligible employees
401(k) for eligible employees
Eligible to participate in short-term incentive programs
AbbVie is a biopharmaceutical company focused on immunology, oncology, neuroscience, virology, and aesthetics. It is a sub-organization of AbbVie.
