Pharma Statistical Programmer (SAS/ADaM)

AbbVie Inc.; North Chicago (IL); On-site; USD 66,000 - 126,000; Full time

Job summary

AbbVie Inc. in North Chicago is seeking a Statistical Programmer to join the research and development team.

You will analyze and report clinical trial data under supervision, interface with statistics, data strategy, medical writing, and regulatory publishing to support regulatory submissions. Responsibilities include creating documentation for regulatory filings, developing SAS macros, consolidating diverse data sources, performing exploratory analyses and visualizations, and validating ADaM

Qualifications

• MS in Statistics, Computer Science or a related field with 0+ years of relevant experience.
• 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 regulatory filing documents (reviewers guides, data definitions).
• Consolidate diverse data sources into analysis-ready datasets.
• Perform exploratory analyses and generate visualizations.
• Develop SAS programs for ADaM data sets per CDISC standards.
• Validate ADaM data sets and Tables, Listings and Figures.

Skills

Communication

Oral and written communication

Education

MS in Statistics, Computer Science or related field

BS in Statistics, Computer Science or related field

Tools

SAS

NONMEM

Job description

AbbVie Inc. in North Chicago is seeking a Statistical Programmer to join the research and development team.

You will analyze and report clinical trial data under supervision, interface with statistics, data strategy, medical writing, and regulatory publishing to support regulatory submissions. Responsibilities include creating documentation for regulatory filings, developing SAS macros, consolidating diverse data sources, performing exploratory analyses and visualizations, and validating ADaM