Senior Specialist, Submission Management Clinical Trials
Bristol Myers SquibbWarsaw, Masovian Voivodeship, Poland
Posted January 30, 2026
116650 - 141347 PLN
Full Time
About the Company
Bristol Myers Squibb is a global biopharmaceutical company dedicated to transforming patients' lives through innovative science. With a strong focus on oncology, hematology, immunology, cardiovascular disease, and fibrosis, the company leverages translational medicine and data analytics to develop personalized therapies. BMS fosters a diverse and inclusive workplace culture, driven by a mission to improve health outcomes for all populations.
Job Description
Working at Bristol Myers Squibb is a unique opportunity to challenge oneself, work on meaningful projects, and contribute to life-changing work. As a Senior Specialist, Submission Management Clinical Trials, you will be responsible for supporting end-to-end regulatory activities for assigned projects, including executing the preparation and compilation of compliant clinical trial maintenance submissions for global health authorities.
Requirements
- BA/BS degree, science/technology field preferred
- 3+ years relevant regulatory submission experience
- Foundational knowledge of global regulatory practices, submission guidelines, and requirements
- Critical thinking and problem-solving skills
- Effective stakeholder engagement and communication
- Proficiency with desktop software and regulatory systems
Benefits
- Competitive benefits, services, and programs
- Wide variety of benefits, including incentive cash and stock opportunities
- Work-life balance and flexibility
- Opportunities for growth and development