Principal Statistical Programmer
3 weeks ago
What you'll be doing:
- 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
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
- Demonstrated working knowledge of advanced SAS macro development and code generation/management algorithms.
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