This role contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions
Job Summary
This role contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
You will drive the design of innovative and efficient clinical trials, develop collaborative relationships, and build the external reputation of BMS.
Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide employees with resources to pursue their goals, both at work and in their personal lives.
Matching Summary
This role 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
regulatory submissions
statistical methodology
Nice-to-have
collaborative relationships
external reputation building
cost-disciplined science
state-of-the-art methodology
Key Requirements
PhD or Master's degree with relevant experience
> 3 years Pharmaceutical/Drug Development experience
Ability to work successfully within cross-functional teams
Excellent verbal and written communications skills