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About the role

Collaborating with cross-functional teams, the full-time Senior Biostatistics Manager will contribute to clinical trial design, protocol development, and regulatory submissions while ensuring high-quality statistical analyses and interpretations.
Key Responsibilities: Collaborates in the design of clinical studies, including methodology and data analysis Authors and reviews protocol documents, statistical analysis plans, and clinical study reports Communicates results and provides data interpretations to cross-functional teamsRequired Qualifications: PhD with 3+ years or MS with 5+ years of experience in statistics or biostatistics Proficiency in scientific computing/programming (SAS, R, or Python) Experience with clinical trials, drug development, or the pharmaceutical industry Familiarity with regulatory requirements and clinical trial design Strong understanding of standard and advanced statistical methods

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JOB OVERVIEW

Experience level

Manager

Location

New York, NY

Occupation

Biostatisticians

Industry

Research and Development in Biotechnology

Posted

yesterday

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