Statistical Analyst - ADaM Programming (Hybrid)

AbbVie•North Chicago, IL

2d•$84,500 - $162,000•Hybrid

About The Position

The Statistical Analyst is an integral role in the research and development of new pharmaceutical products. The role analyzes and reports clinical trial data independently for routine activities and with supervision for more complex activities. The Statistical Analyst interfaces with Statistics, Clinical Data Strategy & Operations, and Development Operations.

Requirements

Master’s degree in Statistics, Computer Science, or a related field and at least 2 years of relevant experience, or bachelor’s degree in one of these fields and at least 4 years of relevant experience.
Experience in pharmaceutical clinical trials.
Demonstrated practical understanding of SAS programming related to drug development.
Experience creating and reviewing ADaM datasets for analysis.
Ability to communicate clearly, both orally and in writing.
Basic understanding of CDISC standards.
Basic understanding of the drug development process.

Nice To Haves

Demonstrated ability to support efficacy analyses across clinical development phases and therapeutic areas.

Responsibilities

Lead statistical programming activities for routine studies.
Create documentation for regulatory filings, including reviewer’s guides and data definition documents.
Participate in developing standard SAS macros and present information on existing macros.
Produce dynamic and static data visualizations to communicate quantitative analyses.
Develop SAS programs to create ADaM datasets following CDISC standards.
Develop SAS programs to create tables, listings, and figures.
Validate ADaM datasets and tables, listings, and figures.
Create specifications for the structure of ADaM datasets for individual studies and integrated data.