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Bristol Myers Squibb is seeking a Manager of Submission Management to lead regulatory activities for clinical trials in Warsaw, Poland. The ideal candidate will have extensive experience in regulatory submissions and people management, with a focus on driving compliance and continuous improvement initiatives.
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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 drive continuous improvement initiatives to enhance efficiencies and ensure consistency across clinical trial applications.
Matching Summary
Match Score: 75
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Bristol Myers Squibb is seeking a Manager of Submission Management to lead regulatory activities for clinical trials in Warsaw, Poland. The ideal candidate will have extensive experience in regulatory submissions and people management, with a focus on driving compliance and continuous improvement initiatives.
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Salary
Base: zł162,775 - zł197,245; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Competitive benefits and programs provided
Skills & Requirements
Must-have
7+ years regulatory submissions experience
People management experience required
Global regulatory practices knowledge
EU CTIS and substantial modifications expertise
English communication proficiency
Nice-to-have
Strategic thinking for complex projects
Innovation in process simplification
Cross-functional stakeholder collaboration
Mentoring and training capabilities
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 guidelines