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.
Key responsibilities include driving the design of innovative and efficient clinical trials, translating scientific questions into statistical terms, and communicating effectively with clinical and regulatory partners.
Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide employees with the 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 as a member of cross-functional development teams.
Skills & Requirements
Must-have
clinical trial design
protocol development
analysis planning
interpretation of results
regulatory submissions
cross-functional team collaboration
Nice-to-have
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