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Overview In this role you will be an experienced clinical programmer leading complex data management activities for trials. You will develop data models, SDTM tabulations, and study-specific reports to support safety, risk, and regulatory submissions. You will ensure
Overview In this role, you develop, verify and document statistical programs to analyze and report clinical data, ensuring timely, high-quality deliverables for projects and submissions. You will be part of a programming team, handling medium to high-complexity
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