Statistical Programmer (Hybrid)

The Statistical Programmer is an integral project team member in the research and development of new pharmaceutical products. Primary responsibilities include 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 the creation of ADaM data sets following CDISC standards.
- Develop SAS programs for the creation of 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 in Statistics, Computer Science, or related field with 2+ years relevant experience.
- Experience with SAS programming.
- Practical experience in other programming languages (e.g., R or Python) preferred.
- Ability to communicate clearly both orally and in writing.

Benefits (as stated):
- Paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees.

Application instructions: None provided.