Clinical SAS Programmer - ADaM & TLF Specialist

Allergan; South San Francisco (CA); On-site; USD 100,000 - 145,000; Full time

Job summary

AbbVie, located in South San Francisco, is seeking a Statistical Programmer to contribute to the analysis and reporting of clinical trial data. You will work under the direction of a Senior Statistical Analyst and interface with Statistics, Data Sciences, and Clinical Operations.

This role emphasizes SAS programming for ADaM data sets and Tables, Listings, and Figures, with emphasis on data standards and regulatory documentation.

Qualifications

• MS in Statistics, Computer Science or a related field with 0+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 2+ years of relevant experience.
• Experience withSAS programming
• Practical experiences in other Programming languages e.g. R or Python is preferred.
• Ability to communicate clearly both oral and written.

Responsibilities

• 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.
• Create documentation for regulatory filings including reviewers guides and data definition documents
• Participate in the development of standard SAS Macros.

Skills

Clear communication

Team collaboration

Education

Master's degree in Statistics/CS

Bachelor's degree in Statistics/CS

Tools

SAS programming

R

Python

Job description

AbbVie, located in South San Francisco, is seeking a Statistical Programmer to contribute to the analysis and reporting of clinical trial data. You will work under the direction of a Senior Statistical Analyst and interface with Statistics, Data Sciences, and Clinical Operations.

This role emphasizes SAS programming for ADaM data sets and Tables, Listings, and Figures, with emphasis on data standards and regulatory documentation.