AbbVie

Create documentation for regulatory filings including reviewers guides and data definition
Participate in the development of standard SAS Macros.
Consolidate heterogeneous data sources (e.g. clinical study databases, external databases
Perform exploratory data analyses and visualizations in interaction with the clinical
Produce dynamic and static data visualizations to communicate quantitative analyses.
Develop SAS programs for the creation of ADaM data sets following CDISC standards.

🎯 Requirements

MS in Statistics, Computer Science or a related field with 0+ years of relevant experience. OR BS
Demonstrated practical understanding of SAS programming and experience with pharmacokinetic (PK)
Ability to communicate clearly both oral and written.
Pharma experience (preferred)

🎁 Benefits

Comprehensive package of benefits including paid time off (vacation, holidays, sick)
Eligible to participate in short-term incentive programs.

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