Senior SAS Programmer

Overview

Perform data manipulation, analysis and reporting of primarily clinical trial data. Create analysis data sets (ADaM & SDTM). Program and generate tables, listings and graphs (TLGs). Validate and document SAS programs and output. Fulfil ad-hoc analysis requests. Other services as needed.

• Perform data manipulation, analysis and reporting of primarily clinical trial data.
• Create analysis data sets (ADaM & SDTM).
• Program and generate tables, listings and graphs (TLGs).
• Validate and document SAS programs and output.
• Fulfil ad-hoc analysis requests.
• Other services as needed.

• Bachelor s degree or equivalent and a minimum of 12+ years of SAS programming experience in the pharmaceutical/biotech industry.
• Strong CDISC experience – ADaM expertise specifically is required.
• Experience interpreting specifications.
• Experience creating source and validation programs using SAS software for ADaM datasets, analysis datasets, and tables, listings, and graphs (TLGs) for multiple studies/products.
• Experience integrating data across multiple studies or drug programs.
• Expertise in the development and use of system-level macro programs.

• Mid-Senior level

• Full-time

• Information Technology

• Biotechnology
• Research and IT Services and IT Consulting

Note:

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