IQVIA in Reading, UK, is hiring a Technical Designer responsible for study build, design, and eCRF configurations within CDMS tools. You will ensure SDTM/CDASH alignment and create/Edit specification documents while coordinating with the DTL, programmers, validation, vendors, statisticians, and client representatives.
The role also covers project financials from the programming shared services perspective and may involve leading essential design meetings to drive successful study delivery.
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Berkshire
In this role you will design and configure study data collection and specifications to support clinical trials, collaborating with cross-functional…
Reading
In this role you will design and configure study data collection and specifications to support clinical trials, collaborating with cross-functional…
London
In this role you lead end-to-end data management for global Phase I–IV trials, focusing on complex oncology, neurology or immunology programs.
London (Feltham)
In this role you lead end-to-end data management for global Phase I–IV trials, focusing on complex oncology, neurology or immunology programs.
United Kingdom
Clinical trials, safety studies, and audits make safe and innovative pharmaceutical-led care possible.
Maidenhead
CSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package.
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