This role contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions as a member of cross-functional development teams
Job Summary
This role contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions as a member of cross-functional development teams.
You will develop collaborative relationships and work effectively with various team members, including the GBDS Biostatistics Lead, medical monitor, and data manager.
Bristol Myers Squibb recognizes the importance of balance and flexibility, offering a wide variety of competitive benefits, services, and programs.
Matching Summary
This role contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions as a member of cross-functional development teams.
Skills & Requirements
Must-have
clinical trial design
protocol development
analysis planning
interpretation of results
regulatory submissions
SAS, R or Python proficiency
applied statistical methodology
Nice-to-have
thought leadership
industry influence
people leadership
novel problem-solving
strategic contribution
collaboration with clinicians
external reputation building
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
Good understanding of regulatory & HTA landscape
Demonstrate collaboration, organizational/ leadership abilities, and interpersonal skills
Demonstrate ability to plan, organize, and prioritize multiple work assignments