Cytel - EMEA
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A leading pharmaceutical services provider is seeking a Tools and Standards Specialist to enhance the Statistical Computing Environment for a major client. The ideal candidate has over 8 years of SAS programming experience and a strong knowledge of CDISC standards. Responsibilities include developing tools for clinical trial reporting and collaborating across teams to drive automation. This role offers the chance to innovate in a dynamic environment.
JOB DESCRIPTION
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 Tools and Standards Specialist 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: This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Tools and Standards Specialist will have a background in Statistical Programming using SAS as well as experience participating and leading in standardization and automation. We are looking for a highly experienced and technically skilled specialist who can convert their knowledge into tools that help make reporting of data from clinical trials and projects more efficient with high quality.
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