Associate Director, Biostatistics

October 28

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Logo of Bristol Myers Squibb

Bristol Myers Squibb

biotechnology • innovation • great place to work • pharmaceuticals • research and development

10,000+

Description

• Contributes to trial design, protocol development, and analysis planning • Manages multiple studies to ensure consistency • Supports health authority requests and public release of information • Authors/reviews protocol, statistical analysis plans, and clinical study reports

Requirements

• PhD (6+ years’ experience) or MS (8+ years’ experience) in statistics or biostatistics or related scientific field • Proficiency in scientific computing/programming (SAS, R or Python) • Great interpersonal, communication, writing and organizational skills • Expertise in statistical/clinical trials methodology • Good understanding of regulatory landscape • Demonstrate collaboration, organizational/leadership abilities

Benefits

• Competitive benefits • Resources to pursue goals at work & personal life

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