Principal Regulatory Affairs Specialist (global Clinical Trial Applications)

Thermo Fisher Scientific

United Kingdom
**
Global regulatory submissions (cta)
Client interfacing
Regulatory agency meetings
** Thermo Fisher Scientific is seeking a Principal Regulatory Affairs Specialist based in the UK, focusing on global clinical trial applications. The role involves leading regulatory strategies for clinical trials, providing regulatory expertise, and collaborating with internal and external clients to ensure compliance and quality. **

Job Summary

  • Lead discussions and coordinate regulatory strategies globally on assigned clinical trials, studies and projects.
  • Act as a representative of the regulatory department with other departments, supporting business development and working on initiatives.
  • Benefit from an award-winning learning and development programme, ensuring you reach your potential.

Matching Summary

Match Score: 75

** Thermo Fisher Scientific is seeking a Principal Regulatory Affairs Specialist based in the UK, focusing on global clinical trial applications. The role involves leading regulatory strategies for clinical trials, providing regulatory expertise, and collaborating with internal and external clients to ensure compliance and quality. **

Skills & Requirements

Must-have

  • Global regulatory submissions (CTA)
  • Client interfacing
  • Regulatory agency meetings

Nice-to-have

  • Innovative solutions
  • Client-focused guidance
  • Quality improvement initiatives

Key Requirements

  • 8+ years of experience
  • Bachelor's degree or advanced degree preferred
  • Knowledge of global clinical trials landscape

Work Rights

Not specified

Tailored Resume

Cover Letter