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Statistical Analyst - ADaM Programming (Hybrid)

AbbVie · Irvine, CA

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Role summary

Statistical Analyst role supporting pharmaceutical research and development through clinical trial data analysis and ADaM programming. Responsibilities include statistical programming for routine studies, SAS development, regulatory documentation, and data validation with hybrid work arrangement in Irvine, CA.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on SmartRecruiters, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-03 (originally posted 2026-10-03). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

  • MS in Statistics, Computer Science, or related field with 2+ years relevant experience; or BS with 4+ years experience
  • Pharmaceutical clinical trials experience
  • Practical SAS programming knowledge for drug development
  • Experience creating and reviewing ADaM datasets
  • CDISC Standards understanding
  • Clear oral and written communication abilities
  • Basic drug development process knowledge

What you'll be doing

  • Lead statistical programming activities for routine clinical studies
  • Develop SAS programs for ADaM dataset creation following CDISC standards
  • Produce Tables, Listings, Figures and data visualizations for quantitative analyses
  • Create regulatory documentation including reviewer guides and data specifications
  • Validate ADaM datasets and analysis outputs for accuracy and compliance

Privacy & handoff

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What RoleLantern checked

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Date posted1 day ago
Last source check1 day ago
Salary listedNeeds clarity
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