Bristol Myers Squibb · Princeton, NJ +1 more
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This senior manager position involves designing clinical trials, developing statistical analysis plans, and interpreting study data within cross-functional teams. The role requires authoring regulatory submissions, communicating findings to stakeholders, and mentoring team members. Candidates should hold a PhD in statistics or biostatistics with 3+ years of experience, or an MS with 5+ years, plus proficiency in SAS, R, or Python.
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