Statistical Programmer

AbbVie

Confirmed live today High trust

Quick summary

Work type
On-site
Location
Irvine, CA
Salary
$65,500–$125,500 / yr
Posted
5 days ago
Freshness
Confirmed live today
Closes
Oct 30, 2126

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $167k
This role $96k
$48k $225k
below market most similar roles pay here above market

This role pays less than 96% of similar roles. Most pay $126,750–$208,147 — the blue band above. At the midpoint, this role pays about $96k versus about $167k for comparable roles.

Based on 240 similar postings.

Employer

About AbbVie

AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines and solutions in immunology, oncology, neuroscience, and eye care. Its products include Humira, Skyrizi, and Rinvoq.

AbbVie currently has 127 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 119 roles with salary data.

Most-posted roles

View all roles at AbbVie

At a glance

TL;DR · Statistical Programmer

The Statistical Programmer serves as an integral project team member in the research and development of new pharmaceutical products. Working under the direction of a Senior Statistical Analyst, the role involves analyzing and reporting clinical trial data while interfacing with stakeholders in Statistics, Clinical Data Strategy and Operations, Medical Writing, Regulatory Publishing, and Development Operations. Key responsibilities include consolidating heterogeneous data sources like clinical study databases and real-world data to prepare analysis-ready sets. The programmer will develop SAS programs for ADaM data sets following CDISC standards, create Tables, Listings, and Figures, and perform exploratory data visualizations. Required skills include practical understanding of SAS programming or NONMEM concepts, creating regulatory documentation, and developing standard SAS Macros to support specific clinical studies.

What you'll do

  • Create documentation for regulatory filings, including reviewer guides and data definition documents.
  • Participate in the development of standard SAS Macros.
  • Consolidate heterogeneous data sources to prepare analysis-ready data sets within a quality control process.
  • Perform exploratory data analyses and visualizations in interaction with clinical pharmacologists or pharmacometricians.
  • Develop SAS programs to create ADaM data sets following CDISC standards.
  • Develop SAS programs for the creation of Tables, Listings, and Figures.
  • Validate ADaM data sets, Tables, Listings, and Figures.
  • Create specifications for the structure of ADaM data sets for individual studies.

What we're looking for

  • Must have an MS in Statistics, Computer Science, or a related field with 0+ years of relevant experience.
  • Must have a BS in Statistics, Computer Science, or a related field with 2+ years of relevant experience.
  • Must have a demonstrated practical understanding of SAS programming or NONMEM concepts and techniques.
  • Must be able to communicate clearly both orally and in writing.

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