Senior Manager 1, Global Submission Management Clinical Trials, Global Regulatory Strategic Operations

Bristor Myers Squibb

Warsaw, Poland
Base: zł251,100 - zł304,272; bonus/equity: + incen...
50% onsite
Global regulatory practices
Clinical trial submissions
Health authority interactions
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 practices
  • Clinical trial submissions
  • Health authority interactions
  • Process simplification initiatives
  • Cross-functional issue resolution

Nice-to-have

  • Innovation promotion
  • Supportive team environment
  • Forward-thinking culture

Key Requirements

  • 7+ years relevant regulatory submissions experience
  • People management experience
  • BA/BS degree, science / technology field preferred
  • Proficient knowledge of global regulatory practices
  • Proficient with desktop software

Work Rights

Not specified

Tailored Resume

Cover Letter