Posted 7 days ago
Description
Bristol Myers Squibb is seeking a Senior SDTM Statistical Programmer to lead SDTM programming for pivotal studies and global regulatory submissions. You will be the technical lead on assigned studies, shaping SDTM strategies from protocol review through to submission, and you will mentor junior programmers and collaborate with CROs.
The role requires 4+ years in pharma/CRO, deep CDISC/SDTM expertise, and strong SAS skills across complex data environments.
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