Sr. Clinical SAS Programmer Job at cGxPServe, Newark, NJ

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  • cGxPServe
  • Newark, NJ

Job Description

Responsibilities:
  • Perform data manipulation, analysis, and reporting of clinical trial data.
  • Develop and maintain department/system-level macros.
  • Create and review SDTM and ADaM specifications.
  • Create and validate SDTM data sets.
  • Create and validate analysis data sets.
  • Create and validate patient profiles.
  • Program and generate tables, figures, and listings (TFLs).
  • Validate and document SAS programs and outputs.
  • Fulfill ad-hoc analysis requests.
  • Provide other services.
Requirements:
  • Bachelor's degree or higher, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, or a related applicable field.
  • Minimum of ten (10) years' SAS programming experience in the pharmaceutical/biotech industry with extensive experience using CDISC standards.
  • Ability to create source and validation programs using SAS software for SDTM datasets, ADaM datasets, and tables, figures, and listings (TFLs) for multiple studies/products.
  • Experience integrating data across multiple studies or drug programs.
  • Expertise in developing and using system-level macro programs.
  • Experience programming with SAS/GTL.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.

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