Statistical Programmer (Hybrid)
AbbVie•Irvine, CA
•Hybrid
About The Position
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.
Requirements
- 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
- Ability to communicate clearly both oral and written.
Nice To Haves
- Practical experiences in other Programming languages e.g. R or Python is preferred.
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.
Benefits
- paid time off (vacation, holidays, sick)
- medical/dental/vision insurance
- 401(k)
- short-term incentive programs
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
