Job Description

Responsibilities:

• Perform data manipulation, analysis, and reporting of clinical trial data.
• Develop and maintain department/system-level macros.
• Create and review SDTM and Adam specifications.
• Create and validate SDTM data sets.
• Create and validate analysis data sets.
• Create and validate patient profiles.
• Program and generate tables, figures, and listings (TFLs).
• Validate and document SAS programs and outputs.
• Fulfil ad-hoc analysis requests.
• Provide other services.

Requirements:

• Bachelor's degree or higher, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, or a related applicable field.
• Minimum of ten (10) years' SAS programming experience in the pharmaceutical/biotech industry with extensive experience using CDISC standards.
• Ability to create source and validation programs using SAS software for SDTM datasets, Adam datasets, and tables, figures, and listings (TFLs) for multiple studies/products.
• Experience integrating data across multiple studies or drug programs.
• Expertise in developing and using system-level macro programs.
• Experience programming with SAS/GTL.
• Proficiency in Microsoft Word, Excel, and PowerPoint.

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