The Associate Director, Biostatistics is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions
Job Summary
The Associate Director, Biostatistics is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
These individuals develop collaborative relationships and work effectively with the GBDS Biostatistics Lead, GBDS medical monitor, protocol manager, data manager, PK scientist, and other members of the study/indication team.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment.
Matching Summary
The Associate Director, Biostatistics is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
Skills & Requirements
Must-have
clinical trial design
protocol development
analysis planning
interpretation of results
regulatory submissions
SAS, R or Python proficiency
Nice-to-have
novel problem-solving
strategic contribution
people leadership
industry influence
thought leadership
Key Requirements
PhD (6+ years’ experience) or MS (8+ years’ experience)
statistics or biostatistics or related scientific field
clinical trials, drug development, pharmaceutical industry, or healthcare experience
Proficiency in scientific computing/programming
Expertise in statistical/clinical trials methodology