Pharma SAS Programmer – ADaM/CDISC Specialist

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

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie is seeking a Statistical Programmer to join our R&D team. You will analyze and report clinical trial data under the direction of a Senior Statistical Analyst and interface with Statistics, Clinical Data Strategy & Operations, Medical Writing, Regulatory Publishing and Development Operations.

The role emphasizes SAS programs for ADaM data sets following CDISC, development of Tables, Listings and Figures, and creation of regulatory data documentation.

Qualifications

• Ability to communicate clearly both oral and written.
• MS or BS with relevant field and experience.
• Demonstrated practical understanding of SAS programming and PK analysis.

Responsibilities

• Create documentation for regulatory filings including reviewers guides and data definition documents.
• Develop SAS macros and data processing processes for analysis-ready datasets.
• Consolidate heterogeneous data sources to prepare analysis-ready data sets for studies.
• Perform exploratory data analyses and visualizations in collaboration with pharmacometricians.
• Produce dynamic and static data visualizations to communicate quantitative analyses.

Skills

Communication

Education

MS in Statistics/CS

BS in Statistics/CS

Tools

SAS

ADaM

Job description

AbbVie is seeking a Statistical Programmer to join our R&D team. You will analyze and report clinical trial data under the direction of a Senior Statistical Analyst and interface with Statistics, Clinical Data Strategy & Operations, Medical Writing, Regulatory Publishing and Development Operations.

The role emphasizes SAS programs for ADaM data sets following CDISC, development of Tables, Listings and Figures, and creation of regulatory data documentation.