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Title:Contract SAS Programmer
Salary:Open
Experience:1+
Location:MA - Cambridge

Description:
Perform validation programming on all assigned studies and responses to requests from regulatory authorities.

Responsibilities:
  • 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.

Requirements:
  • Extensive use of SAS in a pharmaceutical setting
  • Masters degree in Statistics, Biostatistics, Epidemiology, or Computer Science plus one (1) year of experience

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