AbbVie is hiring a Statistical Programmer to support the research and development of new pharmaceutical products. The role analyzes and reports clinical trial data, prepares regulatory documentation and analysis-ready datasets, and develops and validates SAS programs and visualizations in collaboration with cross-functional stakeholders.
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. OR 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
Benefits
Paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 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.
