Ctc-l

Thermo Fisher Scientific UK

Unknown, United Kingdom
2 years relevant experience
Gcp and local regulations knowledge
Ms office proficiency
The role involves supporting audit readiness by ensuring files are reviewed according to the organization's SOP and department guidance

Job Summary

  • The role involves supporting audit readiness by ensuring files are reviewed according to the organization's SOP and department guidance.
  • You will provide administrative support for site activation activities and aid in the development of the critical path for rapid site activations.
  • The position requires maintaining accurate trial status information in databases and ensuring compliance with ICH Good Clinical Practices.

Matching Summary

The role involves supporting audit readiness by ensuring files are reviewed according to the organization's SOP and department guidance.

Skills & Requirements

Must-have

  • 2 years relevant experience
  • GCP and local regulations knowledge
  • MS Office proficiency
  • Strong organizational skills
  • Attention to detail

Nice-to-have

  • Bachelor's degree preferred
  • Local language fluency
  • Team collaboration skills
  • Adaptability to changing timelines
  • Presentation skills

Key Requirements

  • High school diploma or equivalent required
  • Bachelor's degree preferred
  • At least 2 years of relevant experience
  • Knowledge of GCP and applicable SOPs
  • Proficiency in MS Office and clinical trial systems

Work Rights

Not specified

Tailored Resume

Cover Letter