Senior Manager, Submission Management Clinical Trials

Bristol Myers Squibb

50% onsite
7+ years regulatory submissions experience
Global cta dossier preparation
Eu ctis substantial modifications management

Skills & Requirements

Must-have

  • 7+ years regulatory submissions experience
  • Global CTA dossier preparation
  • EU CTIS substantial modifications management
  • Health authority negotiation skills
  • Team leadership and mentoring

Nice-to-have

  • Continuous improvement initiative drive
  • Innovation in regulatory processes
  • Cross-functional stakeholder collaboration
  • Science or technology degree background

Key Requirements

  • BA/BS degree in science/technology field preferred
  • 7+ years relevant regulatory submissions experience
  • Experience managing global clinical trial applications

Work Rights

Not specified

Tailored Resume

Cover Letter