Pharma Statistical Programmer - SAS, ADaM & CDISC

AbbVie; California; On-site; USD 120,000 - 160,000; Full time

Job summary

AbbVie is seeking a Statistical Programmer to support the analysis and reporting of clinical trial data under supervision. The role interfaces with Statistics, Clinical Data Strategy & Operations, Medical Writing, Regulatory Publishing and Development Operations.

Responsibilities include creating regulatory documentation, developing SAS macros, consolidating data sources, and producing analysis-ready data sets and visualizations.

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.
• Develop SAS macros and participate in standard macro development.
• Consolidate heterogeneous data sources to prepare analysis-ready data sets for studies.
• Perform exploratory data analyses and visualizations with clinical pharmacology input.
• Develop SAS programs for ADaM data sets following CDISC standards; create Tables, Listings and Figures.

Skills

SAS programming

NONMEM concepts

Education

MS in Statistics, Computer Science or related field

BS in Statistics, Computer Science or related field with 2+ years

Job description

AbbVie is seeking a Statistical Programmer to support the analysis and reporting of clinical trial data under supervision. The role interfaces with Statistics, Clinical Data Strategy & Operations, Medical Writing, Regulatory Publishing and Development Operations.

Responsibilities include creating regulatory documentation, developing SAS macros, consolidating data sources, and producing analysis-ready data sets and visualizations.