Worldwide Clinical Trials is seeking a skilled Statistical Programmer to join our Global Programming team. You will develop and validate CDISC SDTM/ADaM datasets, create TFLs and listings, and contribute to submission-ready packages across multiple studies.
You will review study specs, lead programming efforts on medium complexity trials, and collaborate with statisticians, sponsors, and programmers to ensure quality and regulatory compliance.
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London
This role will be dedicated to one of IQVIA’s largest clients through a Functional Service Provider (FSP) type partnership.
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