IQVIA LLC in the United Kingdom seeks an experienced CDISC/ SAS programmer to design and drive end-to-end study standards aligned with CDISC and regulatory guidance. You will collaborate with statisticians and programming teams to build global tools and ensure timely, compliant deliverables.
Experts with 10+ years in SAS or equivalent programming, CDISC knowledge, and mentoring ability are preferred. The role emphasizes governance, training, and industry leadership, with a strong focus on
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CDISC Standards Engineer: Regulatory Data & Automation Lead 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.
