AbbVie The Statistical Programmer at AbbVie analyzes and reports clinical trial data under senior oversight. Key duties include developing SAS programs for ADaM data sets and creating documentation for regulatory filings.
Responsibilities
The Statistical Programmer will:
Create documentation for regulatory filings including reviewers guides and data definition documents.
Participate in the development of standard SAS Macros.
The Programmer will:
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
MS in StatisticsOR BS in Statistics
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
