Worldwide Clinical Trials in the United Kingdom is seeking an experienced Statistical Programmer to lead programming efforts on medium to large-scale studies, ensuring CDISC compliance and high-quality outputs.
You will develop and review SDTM/ADaM datasets, TFLs, and deliver analysis-ready data, collaborating with statisticians, sponsors and study teams while advancing SAS expertise across patients and therapies.
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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
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not…
Nottingham
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not…
Nottingham
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not…
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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