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Principal SAS Programmer
Ref No.: 18-15026
Location: Cambridge, Massachusetts
Job Title: Principal SAS Programmer
Duration: 1 year
Location:­ Cambridge, MA

Job Description:

Primary Role:
CLIENT is seeking a Principal SAS Programmer/Manager to contribute to oncology drug development
  • Work with Statistician/CROs to ensure the quality of deliverables TFLs, create/validate SDTM/ADaM specs and QC SDTM mapping/ ADaM datasets / TFLs.   
  • Provide in-house programming supports such as ad-hoc analysis, CSR programming, regulatory filings, publication requests.
  • Contribute to develop/validate SAS programming of endpoints based on RECIST criteria.
  • Review clinical study documents including CRF design/Annotation, SDTM specs, and edit checks and contribute to data cleaning process.
  • Support creation and validation of esubmission requirements (i.e. annotated CRF, data export files, define documents).
  • Contribute to SOP development for programming and validation process, in-house infrastructure of programming (folder structure/Data achieving/Central File Maintenance. )
  • Contribute to develop SAS programming standard templates of ADaM/TFLs and other statistical documents.
  • Contribute to data pooling of integrated summary of Safety (ISS) / Efficacy (Client).
  • Familiar with SDTM, ADaM, and CDISC/eSub requirements for regulatory submissions.
  • Expertise in SAS programming/Macro development.
  • Experience with data pooling to support Integrated Summary of Safety (ISS) / Efficacy (Client) preferred.
  • Ability of handle multiple tasks with multiple timelines.
  • Excellent inter-personal skills in management, collaboration and communication internally and externally.
  • Management Experience as coordinating programming activities.
  • MS with seven years' experience including industry background.
  • Oncology experience preferred.
Shiva Prasad | Senior Recruiter
Sunrise Systems Inc.
Desk: (732) 272 0346
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