Responsibilities:
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.
Requirements:
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.
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