Hybrid Statistical Analyst — Pharma Data & SAS Expert

ABBVIE

South San Francisco (CA)

On-site

USD 85,000 - 162,000

Full time

46 hours ago

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Benefits offered by this job

401(k) plan

Paid time off

Medical/dental/vision insurance

Job summary

AbbVie in South San Francisco, CA, is seeking a Statistical Analyst to support the research and development of new medicines. You will lead statistical programming activities for routine studies and prepare documentation for regulatory filings, working with cross‑functional teams across Statistics, Clinical Data Strategy & Operations and Development Operations.

The ideal candidate has a MS or BS in Statistics, Computer Science or related field with several years’ experience in pharmaceutical

Qualifications

MS or BS in Statistics, Computer Science or a related field with 2+ or 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