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Senior Statistical Programmer FSP at Cytel. Location Information: United Kingdom. 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 Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. . Position Overview: . As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote. . Our values. . We believe in applying scientific rigor to reveal the full promise inherent in data.. . We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.. . We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.. . We prize innovation and seek intelligent solutions using leading-edge technology.. . . How you will contribute:. . . . Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming. . Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs). . Production and QC / validation programming. . Generating complex ad-hoc reports utilizing raw data. . Applying strong understanding/experience of Efficacy analysis. . Creating and reviewing submission documents and eCRTs. . Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries. . Performing lead duties when called upon. . Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.. . Being adaptable and flexible when priorities change. . . . . . Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have: . . Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.. . At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above.. . Study lead experience, preferably juggling multiple projects simultaneously preferred.. . Strong SAS data manipulation, analysis and reporting skills.. . Solid experience implementing the latest CDISC SDTM / ADaM standards.. . Strong QC / validation skills.. . Good ad-hoc reporting skills. . . Proficiency in Efficacy analysis.. . Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.. . Submissions experience utilizing define.xml and other submission documents.. . Experience supporting immunology, respiratory or oncology studies would be a plus.. . Excellent analytical & troubleshooting skills.. . Ability to provide quality output and deliverables, in adherence with challenging timelines.. . Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.. . .