Job Summary
Perform role of primary or validation programmer to generate Tables, Figures and Listings (TFLs) on all assigned
studies and responses to requests from regulatory authorities.
Job Description
- Perform role of validation programmer on all assigned studies and responses to requests from regulatory authorities.
- Review data definition tables for SDTM and derived data sets for assigned studies and provide comments.
- Review data definition tables for SDTM and derived data sets for assigned partner studies and provide comments.
- Review statistical analysis plans for all assigned studies in conjunction with primary study statistical programmer
and provides comments to study biostatistician.
- Review annotated case report forms in conjunction with primary study statistical programmer and provides comments to
study database administrator.
- Review edit check specifications in conjunction with primary study statistical programmer and provide comments to study data manager.
- Support direct supervisor and Senior/Director, Statistical Programming.
Job Requirements
Education: Bachelors Degree in Statistics, Biostatistics, Epidemiology, or Computer Science.
Experience: Two (2) years experience performing statistical programming using SAS® in a pharmaceutical setting, or equivalent.
Knowledge, Skills, and Abilities
- Must know basics of programming with SAS®.
- Strong oral and written communication skills.
