Hybrid Statistical Analyst for Pharma Data & SAS

Allergan; Florham Park (NJ); On-site; USD 90,000 - 120,000; Full time

Job summary

AbbVie in Florham Park, NJ is seeking a Statistical Analyst to support the research and development of new pharmaceutical products. You will analyze and report clinical trial data with minimal supervision for routine tasks and collaborate with Statistics, Clinical Data Strategy & Operations, and Development Operations.

The role requires strong SAS programming skills, experience with ADaM datasets and CDISC standards, and the ability to present findings clearly in writing and verbally.

Qualifications

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

Skills

SAS programming

ADaM datasets

CDISC standards

Data visualization

Regulatory documentation

Education

MS in Statistics/CS

BS in Statistics/CS

Tools

SAS Macros

Job description

AbbVie in Florham Park, NJ is seeking a Statistical Analyst to support the research and development of new pharmaceutical products. You will analyze and report clinical trial data with minimal supervision for routine tasks and collaborate with Statistics, Clinical Data Strategy & Operations, and Development Operations.

The role requires strong SAS programming skills, experience with ADaM datasets and CDISC standards, and the ability to present findings clearly in writing and verbally.