Clinical Statistical Programmer - SAS & ADaM

AbbVie Inc.; Irvine (CA); On-site; USD 90,000 - 130,000; Full time

Job summary

AbbVie Inc. is seeking a Statistical Programmer to support R&D analytics for clinical trials. You will analyze and report data under supervision, interfacing with Statistics, Clinical Data Strategy & Operations, Medical Writing, and Regulatory teams.

The role emphasizes developing ADaM data sets, creating Tables, Listings and Figures, and building regulatory-grade documentation for filings. Strong communication is essential to success.

Qualifications

• MS in Statistics, Computer Science or a related field with 0+ years of relevant experience, or BS with 2+ years of 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.
• Contribute to development of SAS Macros and standards.
• Consolidate heterogeneous data sources to prepare analysis-ready data sets and perform exploratory analyses.
• Develop SAS programs for ADaM data sets, Tables, Listings and Figures; validate outputs.

Skills

SAS programming

NONMEM concepts

Communication skills

Education

MS in Statistics, Computer Science or related field

BS in Statistics, Computer Science or related field

Tools

SAS Macros

SAS

Job description

AbbVie Inc. is seeking a Statistical Programmer to support R&D analytics for clinical trials. You will analyze and report data under supervision, interfacing with Statistics, Clinical Data Strategy & Operations, Medical Writing, and Regulatory teams.

The role emphasizes developing ADaM data sets, creating Tables, Listings and Figures, and building regulatory-grade documentation for filings. Strong communication is essential to success.