IQVIA in Reading, United Kingdom, is seeking a senior statistician/programmer to develop end-to-end CDISC standards and study specifications that align with FDA guidance. You will work with project statisticians and programming teams to build global tools and lead productivity initiatives in CDISC compliance.
The role emphasizes mentoring others, governance of CDISC standards, and staying current with regulatory updates, with responsibilities spanning client collaboration, training, and industry
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CDISC Standards Engineer & Automation Lead in Reading employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.
