Clinical Trial Reg Affairs Specialist Iii

Thermo Fisher Scientific UK

Remote
Regulatory compliance
Project management
Documentation preparation
Supports the preparation of documentation and submissions under EUCTR guidance

Job Summary

  • Supports the preparation of documentation and submissions under EUCTR guidance.
  • Coordinates and manages client deliverables supporting regulatory compliance.
  • Maintains knowledge and understanding of SOPs and current regulatory guidelines.

Matching Summary

Supports the preparation of documentation and submissions under EUCTR guidance.

Skills & Requirements

Must-have

  • regulatory compliance
  • project management
  • documentation preparation

Nice-to-have

  • client liaison skills
  • data analysis
  • team collaboration

Key Requirements

  • Bachelor's or master’s degree
  • 4+ years of relevant experience

Work Rights

Not specified

Tailored Resume

Cover Letter