Bristol Myers Squibb is seeking a Director of Biostatistics to lead statistical support for clinical trials and drug development. This role involves innovative study design, team management, and collaboration with cross-functional teams to ensure high-quality deliverables, contributing to the company's mission of transforming patients’ lives through science
Job Summary
Director of Biostatistics is a member of cross-functional team and contributes to development of compounds within a therapeutic area.
Presents and defends complex statistical solutions to all levels of BMS governance, key stakeholders and external regulatory bodies in a clear, concise, complete, and transparent manner that provide influence on key decisions.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment.
Matching Summary
Match Score: 85
Bristol Myers Squibb is seeking a Director of Biostatistics to lead statistical support for clinical trials and drug development. This role involves innovative study design, team management, and collaboration with cross-functional teams to ensure high-quality deliverables, contributing to the company's mission of transforming patients’ lives through science.
Salary
Base: $218,740 - $265,060; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Paid Time Off
Skills & Requirements
Must-have
clinical trials, drug development
scientific and strategic partner
statistical solutions to governance
health authority request support
adherence to global and project standards
functional or project budget management
Nice-to-have
inclusive culture, diversity
human touch to every treatment
collaboration, innovation, productivity
Key Requirements
PhD (9+ years) or MS (11+ years) in statistics or biostatistics
Proficiency in scientific computing/programming (SAS, R or Python)
Excellent interpersonal, communication, writing and organizational skills
Experience in preparing and participating in global regulatory agency interactions
At least 3 years management (direct or matrix) experience preferred