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Principal Programmer Single Sponsor
1 month ago
- Ideally you will have knowledge in all aspects of clinical trials, from initial study set-up to study completion, with an understanding of the roles and responsibilities of all related disciplines, e.g. Biostatistics and Clinical Data Management
- Expert knowledge of base SAS, SAS macros, SAS/STAT and in debugging SAS programs
- Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml, Reviewer's Guides and submission standards
- An autonomous, collaborative work style, a curious mind and a keen attention to detail
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