Manager I, Submission Management Clinical Trials

Bristor Myers Squibb

Warsaw, Poland
Base: zł162,775 - zł197,245; bonus/equity: + incen...
50% onsite
Clinical trial submissions
Regulatory standards
Health authority interactions
The Manager, Submission Management Clinical Trials supports end-to-end regulatory activities for assigned projects, including leading the preparation and compilation of compliant clinical trial submissions for global health authorities and supporting continuous improvement initiatives

Job Summary

  • The Manager, Submission Management Clinical Trials supports end-to-end regulatory activities for assigned projects, including leading the preparation and compilation of compliant clinical trial submissions for global health authorities and supporting continuous improvement initiatives.
  • Collaborate with global and local stakeholders to define clinical trial submission strategies and document requirements, ensuring alignment with regulatory standards and project timelines.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

The Manager, Submission Management Clinical Trials supports end-to-end regulatory activities for assigned projects, including leading the preparation and compilation of compliant clinical trial submissions for global health authorities and supporting continuous improvement initiatives.

Salary

Base: zł162,775 - zł197,245; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Competitive benefits, services and programs

Skills & Requirements

Must-have

  • clinical trial submissions
  • regulatory standards
  • health authority interactions
  • CTIS data management
  • Veeva RIM system proficiency

Nice-to-have

  • innovation and process simplification
  • AI and automation tools
  • cross-functional alignment
  • patient life transformation

Key Requirements

  • BA/BS degree, science / technology field preferred
  • 3+ years relevant regulatory submissions experience
  • Proficient knowledge of global regulatory practices
  • Strong analytical and critical thinking skills
  • Effective communication skills in English
  • Solid project management abilities
  • Build collaborative relationships
  • Advanced proficiency with desktop software and regulatory systems

Work Rights

Not specified

Tailored Resume

Cover Letter