SAS Programmer III

4 weeks ago

Basking Ridge, United States Katalyst Healthcares and Life Sciences Full time
Responsibilities:
  • Perform SDTM mapping and create SDTM annotated CRF.
  • Create SDTM domain specifications and develop/update SDTM company standard specifications.
  • Develop SDTM domain based on SDTM specifications or perform programmatic review of study SDTM domains generated by vendor and ensure SDTM deliverable quality.
  • Provide CDISC SDTM expertise to study team and ensure CDISC compliance in DS submission SDTM data package.
  • Support building compound SDTM programming convention.
  • Maintain institutional knowledge from DS SDTM history, and support building up programming standard on SDTM to improve efficiency and quality.
  • Develop and manage CRO to ensure SDTM programming support with efficiency, quality and completeness
Requirements:
  • Must have at least 5+ years of strong SDTM Study Data Tabulation Model (SDTM) development and programming skills.
  • Knowledge in clinical trials with 5+ years' experience working in a clinical project team environment meeting deadlines with quality deliverables.
  • SAS experience in major pharma or CRO.
  • Proficient computer skills across multiple applications and OS environments.
  • Experience developing and working with company SDTM standards. Experiences working with CRO vendor.

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