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 to create 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 of relevant experience; OR BS with 2+ years of relevant experience.
- Experience with SAS programming.
- Practical experience with other programming languages (e.g., R or Python) preferred.
- Ability to communicate clearly both orally and in writing.

Benefits (if explicitly stated):
- Paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees.
- Eligible for short-term incentive programs.