Clinical SAS Programmer - ADaM & Data Visualization

AbbVie; North Chicago (IL); On-site; USD 85,000 - 110,000; Full time

Job summary

AbbVie seeks a Statistical Programmer to join the R&D team in the development and analysis of clinical trial data. The role involves creating regulatory documentation, developing SAS macros, and consolidating diverse data sources to produce analysis-ready datasets in ADaM format following CDISC standards.

You will perform exploratory analyses, generate visualizations, and validate ADaM datasets and TLFs, collaborating with statisticians, data strategy, medical writing, and regulatory teams.

Qualifications

• MS in Statistics, Computer Science or a related field with 0+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 2+ years of relevant experience.
• Demonstrated practical understanding of SAS programming or NONMEM concepts and techniques.
• Ability to communicate clearly both oral and written.

Responsibilities

• Create documentation for regulatory filings including reviewers guides and data definition documents.
• Participate in the development of standard SAS Macros.
• Consolidate heterogeneous data sources (e.g. clinical study databases, external databases, real-world data) to prepare analysis-ready data sets within a defined quality control process supporting a particular study.
• Perform exploratory data analyses and visualizations in interaction with the clinical pharmacologist or pharmacometrician.
• Produce dynamic and static data visualizations to communicate quantitative analyses.
• Develop SAS programs for the creation of ADaM data sets following CDISC standards
• Develop SAS programs for the creation of Tables, Listings and Figures.
• Validation of ADaM data sets.
• Validation of Tables, Listings and Figures.
• Create specifications for the structure of ADaM data sets for individual studies.

Skills

SAS programming

NONMEM concepts

Communication

Education

MS in Statistics/CS/related

BS in Statistics/CS/related

Tools

SAS

CDISC ADaM

TLFs (Tables, Listings & Figures)

Job description

AbbVie seeks a Statistical Programmer to join the R&D team in the development and analysis of clinical trial data. The role involves creating regulatory documentation, developing SAS macros, and consolidating diverse data sources to produce analysis-ready datasets in ADaM format following CDISC standards.

You will perform exploratory analyses, generate visualizations, and validate ADaM datasets and TLFs, collaborating with statisticians, data strategy, medical writing, and regulatory teams.