Statistical Analyst, ADaM & SAS (Hybrid)

SmartRecruiters, Inc.; Irvine (CA); Hybrid; USD 85,000 - 162,000; Full time

Job summary

AbbVie in Irvine, CA is seeking a Statistical Analyst for ADaM programming in a hybrid role. You will lead SAS programming activities for routine studies, develop ADaM datasets and create regulatory documentation, while collaborating with Statistics and Clinical Data Strategy teams.

The role requires 2+ years (MS) or 4+ years (BS) in stats/compsci, pharma trials, SAS proficiency, and CDISC ADaM experience. Competitive compensation is disclosed and a comprehensive benefits package is offered.

Qualifications

• MS in Statistics, Computer Science or a related field with 2+ years of relevant experience.
• BS in Statistics, Computer Science or a related field with 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

Responsibilities

• Leads the statistical programming activities for routine studies.
• Create documentation for regulatory filings including reviewers guides and data definition documents
• Participate in the development of standard SAS Macros, as well as, presenting information on existing Macros
• Produce dynamic and static data visualizations to communicate quantitative analyses.
• Develop SAS programs for the creation of ADaM data sets following CDISC standards.
• Develop SAS programs for the creation of Tables, Listings and Figures.
• Validation of ADaM data sets. Validation of Tables, Listings and Figures.
• Create specifications for the structure of ADaM data sets for individual studies and integrated data

Skills

Experience in pharmaceutical trials

SAS programming

ADaM datasets experience

Oral and written communication

Education

MS in Statistics / Computer Science or related

BS in Statistics / Computer Science or related

Tools

SAS

Job description

AbbVie in Irvine, CA is seeking a Statistical Analyst for ADaM programming in a hybrid role. You will lead SAS programming activities for routine studies, develop ADaM datasets and create regulatory documentation, while collaborating with Statistics and Clinical Data Strategy teams.

The role requires 2+ years (MS) or 4+ years (BS) in stats/compsci, pharma trials, SAS proficiency, and CDISC ADaM experience. Competitive compensation is disclosed and a comprehensive benefits package is offered.