Statistical Programmer (Hybrid)

The Statistical Programmer is an integral project team member in the research and development of new pharmaceutical products. Primary responsibilities include the analysis and reporting of clinical trial data under the direction and oversight of a Senior Statistical Analyst. Interfaces with Statistics, Data Sciences and Clinical Operations.

Job Responsibilities:
- Develop SAS programs for creation of ADaM data sets following CDISC standards.
- Develop SAS programs for 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.
- Create documentation for regulatory filings, including reviewer guides and data definition documents.
- Participate in the development of standard SAS Macros.

Qualifications:
- MS in Statistics, Computer Science or related field with 0+ years relevant experience. OR BS with 2+ years relevant experience.
- Experience with SAS programming.
- Practical experience in other languages (e.g., R or Python) preferred.
- Ability to communicate clearly (oral and written).