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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Reading
IQVIA in Reading, United Kingdom, is seeking a senior statistician/programmer to develop end-to-end CDISC standards and study specifications that…
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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…
Reading
IQVIA in Reading, UK seeks a senior CDISC Standards expert to lead end-to-end design of client standards and study specifications aligned to CDISC…
Reading
This position is responsible for the development of the end-to-end design of client standards and study specifications that align to the CDISC…
Reading
This position is responsible for the development of the end-to-end design of client standards and study specifications that align to the CDISC…
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