Clinical SAS Programmer Job at cGxPServe, Irving, TX

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  • cGxPServe
  • Irving, TX

Job Description

Responsibilities:
  • Performing data manipulation, analysis, and reporting of clinical trial data for both safety and efficacy (ISS/Client) utilizing SAS programming.
  • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs).
  • Production and QC / validation programming.
  • Ability to program from scratch and able to handle complicated domains and TLF's. Ability to read and apply protocol and SAP.
  • Demonstrate good understanding of the endpoints and data collection.
  • Generating complex ad-hoc reports utilizing raw data.
Requirements:
  • Bachelor's degree in one of the following fields Statistics, Computer Science, Mathematics, or related field.
  • At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent. At least 6 years of related experience with a master's degree or above.
  • Study lead experience, preferably juggling multiple projects simultaneously preferred.
  • Strong SAS data manipulation, analysis, and reporting skills.
  • Solid experience implementing the latest CDISC SDTM / ADaM standards.
  • Strong QC / validation skills.
  • Proficiency in Efficacy analysis.
  • Ability to provide quality output and deliverables in adherence with challenging timelines.
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

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