Senior/Principal Statistical Programmer SAS + R (Remote) Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our general pharmaceutical clients;
The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.
Xml files for multiple studies
+ Develop SAS programs which generate datasets, complex listings,



tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs
+ Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs
+ Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines
+ Understand and follow FDA regulations which affect the reporting of clinical trial data. Participate in the development of CRFs, edit check specifications, and data validation plans
+ Provide review and/or author data transfer specifications for external vendor data
+ CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals
+ Here at Cytel we want our employees to succeed and we enable this success through consistent training, development a

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