Fsp Sr Cra

Thermo Fisher Scientific UK

Beijing, China
Regulatory strategy advice
Clinical trial monitoring
Site activation management
The role involves preparing and coordinating local regulatory submissions in alignment with global strategies

Job Summary

  • The role involves preparing and coordinating local regulatory submissions in alignment with global strategies.
  • You will serve as the primary contact for investigators and local regulatory authorities to ensure timely submissions.
  • The position requires developing country-specific documents and managing site start-up activities effectively.

Matching Summary

The role involves preparing and coordinating local regulatory submissions in alignment with global strategies.

Skills & Requirements

Must-have

  • Regulatory strategy advice
  • Clinical trial monitoring
  • Site activation management

Nice-to-have

  • Effective communication skills
  • Project management experience
  • Team collaboration

Key Requirements

  • Bachelor's degree
  • 4+ years as a clinical research monitor

Work Rights

Not specified

Tailored Resume

Cover Letter