Statistical Programmer (Hybrid)

The Statistical Programmer is an integral project team member in the research and development of new pharmaceutical products, analyzing and reporting 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 to create 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:
Minimum Qualifications
- MS in Statistics, Computer Science or a related field with 0+ years of relevant experience. OR BS with 2+ years of relevant experience.
- Experience with SAS programming.
- Practical experience in other programming languages (e.g., R or Python) is preferred.
- Ability to communicate clearly, oral and written.

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