Support end-to-end regulatory activities for assigned projects, including leading the preparation and compilation of compliant clinical trial submissions for global health authorities
Job Summary
Support end-to-end regulatory activities for assigned projects, including leading the preparation and compilation of compliant clinical trial submissions for global health authorities.
Drive initiatives that promote innovation and simplify processes to enhance efficiencies for BMS teams and ensure consistency of Clinical Trial Applications across projects, studies, and countries.
Be a key leader in global studies impacting diverse therapeutic areas and grow your career in a supportive, forward-thinking environment.
Matching Summary
Support end-to-end regulatory activities for assigned projects, including leading the preparation and compilation of compliant clinical trial submissions for global health authorities.
Salary
Base: zł251,100 - zł304,272; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Not specified
Skills & Requirements
Must-have
global regulatory strategic operations
clinical trial submissions
health authority submissions
regulatory requirements maintenance
cross-functional issue resolution
Nice-to-have
driving innovation and simplification
supportive forward-thinking environment
transforming patients' lives through science
Key Requirements
7+ years relevant regulatory submissions experience
people management experience
BA/BS degree, science / technology field preferred
Proficient knowledge of global regulatory practices