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Statistical Analyst - ADaM Programming (Hybrid)

AbbVie · South San Francisco, CA

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Role summary

AbbVie seeks a Statistical Analyst to support clinical trial data analysis and ADaM programming for pharmaceutical development. The role involves statistical programming leadership for routine studies, regulatory documentation, SAS program development, and data validation in a hybrid South San Francisco position.

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 Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.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
  • Pharmaceutical clinical trial experience
  • Demonstrated practical SAS programming knowledge for drug development
  • Experience creating and reviewing ADaM datasets for analysis
  • Basic understanding of CDISC Standards
  • Clear oral and written communication skills
  • Basic understanding of drug development process

What you'll be doing

  • Lead statistical programming activities for routine clinical studies
  • Develop SAS programs for ADaM dataset creation following CDISC standards
  • Create and validate Tables, Listings, and Figures from clinical data
  • Produce regulatory documentation including reviewers guides and data definition documents
  • Develop standard SAS Macros and present information on existing macro functionality

Privacy & handoff

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Date posted1 day ago
Last source check1 day ago
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