Job Description

• Client has an urgent need for a statistical programmer with extensive validation experience. Will be validating SDTMs and ADaMs produced by CRO via independent programming
• Must have extensive risk-based validation experience
• Early development experience preferred
• Review SDTM and ADaM specifications in details. Must be able to understand the protocol and SAP when reviewing the programming specifications.
• Familiarity with clinical trial design and analysis activities. Strong knowledge of CDISC SDTM and ADaM data models
• Strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat, and SAS Macros
• Exceptional organizational and time management skills, with the ability to multi-task
• Min. 8 years hands on statistical programming experience in the pharma/biotech in

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