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Urgent! Sr. Clinical SAS Programmer Job Opening In Newark – Now Hiring Katalyst HealthCares & Life Sciences

Sr. Clinical SAS Programmer



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 () 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.



  • Required Skill Profession

    Computer Occupations



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