SAS-Driven Pharma Statistical Programmer (ADaM/CDISC)

ABBVIE; Florham Park (NJ); On-site; USD 66,000 - 126,000; Full time

Job summary

AbbVie in Florham Park, NJ is seeking a Statistical Programmer to join the R&D team. The role focuses on analysis and reporting of clinical trial data under supervision of a Senior Statistical Analyst, interfacing with Statistics, Data Sciences and Clinical Operations.

Responsibilities include developing SAS programs to create ADaM data sets per CDISC, generating Tables, Listings and Figures, validating outputs, drafting study specifications and data definitions for regulatory filings.

Qualifications

• MS in Statistics, Computer Science or a related field with 0+ years of relevant experience
• BS in Statistics, Computer Science or a related field with 2+ years of relevant experience
• Experience with SAS 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

SAS programming

R or Python

Clear communication

Education

MS in Statistics/Computer Science or related

BS in Statistics/Computer Science or related with 2+ years

Job description

AbbVie in Florham Park, NJ is seeking a Statistical Programmer to join the R&D team. The role focuses on analysis and reporting of clinical trial data under supervision of a Senior Statistical Analyst, interfacing with Statistics, Data Sciences and Clinical Operations.

Responsibilities include developing SAS programs to create ADaM data sets per CDISC, generating Tables, Listings and Figures, validating outputs, drafting study specifications and data definitions for regulatory filings.