Senior Biostatistical Programmer

Responsibilities

• Develops SAS programs to generate listings, tables and figures as outlined by mock TLF shells
• Performs quality control (source code review, double-programming and log review) of SAS programs
• Develops SAS programs to generate CDISC and other analysis data sets as outlined by respective specifications
• Prepares specifications for CDISC and other analysis data sets
• Assists Data Management with SAS programming needs
• Acts as Lead Biostatistical Programmer to interact with the Lead Biostatistician and the study team
• Develops and validates general SAS macros
• What we are searching for:
• BS or equivalent from accredited college or university, in statistics, IT, mathematics or closely related field or work related experience to be able to perform this role
• 6-8 years of experience in SAS programming within the area of clinical trials.
• Prior experience using computerized information systems preferred.
• Knowledge of ICH and local regulatory authority drug research and development regulations preferred.
• Advanced knowledge of SAS Software data set architecture, utilities, and programming techniques

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Company Intel

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