Manager, Submission Management

Bristol Myers Squibb

Warsaw, Poland
Base: zł162,775 - zł197,245; bonus/equity: + incen...
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7+ years regulatory submissions experience
People management and team leadership
Global clinical trial submission strategies
** Bristol Myers Squibb is seeking a Senior Manager for Submission Management in Warsaw, Poland, to oversee regulatory activities for clinical trials. The ideal candidate should possess extensive experience in regulatory submissions and team leadership, with a strong emphasis on compliance and continuous improvement. **

Job Summary

  • This role involves leading the preparation and compilation of compliant clinical trial submissions for global health authorities.
  • The position offers a hybrid work model allowing up to 50% remote work over a two-week period with flexible scheduling.
  • Candidates will collaborate with high-achieving teams across the US, India, Switzerland, and beyond to shape the future of clinical trials.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Senior Manager for Submission Management in Warsaw, Poland, to oversee regulatory activities for clinical trials. The ideal candidate should possess extensive experience in regulatory submissions and team leadership, with a strong emphasis on compliance and continuous improvement. **

Salary

Base: zł162,775 - zł197,245; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs

Skills & Requirements

Must-have

  • 7+ years regulatory submissions experience
  • People management and team leadership
  • Global clinical trial submission strategies
  • EU CTIS and substantial modifications knowledge
  • Stakeholder negotiation and query management

Nice-to-have

  • Continuous improvement initiative drive
  • Cross-functional collaboration skills
  • Strategic thinking for complex projects
  • Innovation in regulatory processes
  • Mentoring and training new staff

Key Requirements

  • BA/BS degree in science or technology field
  • 7+ years relevant regulatory submissions experience
  • Proven people management experience
  • Proficient knowledge of global regulatory practices

Work Rights

Not specified

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