Senior Manager, Global Clincal Science - Cardiovascular

Bristol Myers Squibb

Warsaw, Poland
Base: zł328,440 - zł397,992; bonus/equity: + incen...
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Design and execution of clinical trials
Knowledge of gcp/ich guidelines
Protocol and icf document development
** Bristol Myers Squibb is seeking a Senior Manager for Global Clinical Science focused on Cardiovascular projects in Warsaw, Poland. The ideal candidate will be responsible for designing and executing clinical trials, collaborating with external partners, and ensuring compliance with clinical documentation standards. **

Job Summary

  • The role involves designing and executing clinical trial activities while collaborating closely with cross-functional teams to conduct cardiovascular studies.
  • Candidates will be responsible for developing protocol documents, reviewing clinical data for trends, and contributing to regulatory submissions.
  • Bristol Myers Squibb offers a supportive culture with competitive benefits and opportunities for career growth alongside high-achieving teams.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Senior Manager for Global Clinical Science focused on Cardiovascular projects in Warsaw, Poland. The ideal candidate will be responsible for designing and executing clinical trials, collaborating with external partners, and ensuring compliance with clinical documentation standards. **

Salary

Base: zł328,440 - zł397,992; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs provided

Skills & Requirements

Must-have

  • Design and execution of clinical trials
  • Knowledge of GCP/ICH guidelines
  • Protocol and ICF document development
  • Data review and trend identification
  • Medical writing skills

Nice-to-have

  • Experience with KOL collaboration
  • Cross-functional team leadership
  • Intermediate critical thinking skills
  • Project management capabilities

Key Requirements

  • Degree in Life Sciences (MD, PhD, Pharm D, MS, RN)
  • Basic knowledge of drug development process and study design
  • Intermediate medical writing skills

Work Rights

Not specified

Tailored Resume

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