Statistical Programmer (Hybrid)

Job description

The Statistical Programmer is an integral project team member in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data under the direction and oversight of a Senior Statistical Analyst. The Statistical Programmer interfaces with Statistics, Data Sciences and Clinical Operations. Job Responsibilities: • 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. • Create documentation for regulatory filings including reviewers guides and data definition documents • Participate in the development of standard SAS Macros. Minimum Qualifications • 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. • Experience with SAS programming • Practical experiences in other Programming languages e.g. R or Python is preferred. • Ability to communicate clearly both oral and written. About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.