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Statistical Analyst - ADaM Programming (Hybrid)

AbbVie · Florham Park, NJ

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Role summary

Statistical Analyst role focused on ADaM programming and clinical trial data analysis for pharmaceutical research and development. Responsibilities include leading statistical programming activities, creating regulatory documentation, developing SAS programs for datasets and reports, and validating analyses.

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 Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.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

What you'll be doing

  • Lead statistical programming activities for routine clinical studies
  • Develop SAS programs to create ADaM datasets following CDISC standards
  • Create specifications for ADaM dataset structure for individual and integrated studies
  • Produce Tables, Listings, Figures and data visualizations to communicate analyses
  • Validate ADaM datasets and create regulatory documentation including reviewers guides

Privacy & handoff

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