CSL Vifor in Maidenhead seeks a Senior Clinical Statistical Programmer to own one or two trials from first line of code to submission-ready package. You will design, validate SDTM/ADaM datasets and outputs, work with statisticians and data managers, and mentor junior programmers.
You will lead end-to-end programming across the study lifecycle, review CRO deliverables, and ensure audit-ready analyses and documentation for regulatory submission.
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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.
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.
Nottingham
Worldwide Clinical Trials is seeking a skilled Statistical Programmer to join our Global Programming team.
Nottingham
Worldwide Clinical Trials is seeking a skilled Statistical Programmer to join our Global Programming team.
Nottingham
Worldwide Clinical Trials in the United Kingdom is seeking an experienced Statistical Programmer to lead programming efforts on medium to…
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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