Hybrid Statistical Analyst - ADaM & SAS for Pharma

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

Job summary

AbbVie in South San Francisco is seeking a Statistical Analyst specialized in ADaM programming to support drug development efforts. The role provides hybrid work options and focuses on delivering robust programming for ADaM datasets, tables, listings and figures.

You will lead programming for routine studies, create regulatory documentation, and develop SAS macros while ensuring CDISC standards. Strong communication and collaboration with biostatistics teams are essential.

Qualifications

• MS in Statistics, Computer Science or related field with 2+ years of relevant experience, OR BS with 4+ years of relevant experience.
• Experience in pharmaceutical clinical trials.
• Practical SAS programming experience 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 and Tables/Listings/Figures.
• Create specifications for the structure of ADaM data sets for individual studies and integrated data.

Skills

Statistical analysis

SAS programming

Clinical trials

Education

MS in Statistics

BS in Statistics

Tools

SAS

CDISC

ADaM

Job description

AbbVie in South San Francisco is seeking a Statistical Analyst specialized in ADaM programming to support drug development efforts. The role provides hybrid work options and focuses on delivering robust programming for ADaM datasets, tables, listings and figures.

You will lead programming for routine studies, create regulatory documentation, and develop SAS macros while ensuring CDISC standards. Strong communication and collaboration with biostatistics teams are essential.