Clinical Trial Coordinator - Veeva Etmf (night Shift/remote)

Thermo Fisher Scientific UK

Etmf system proficiency
Site activation critical path
Ich gcp knowledge
The role involves providing administrative and technical support to ensure audit readiness and rapid site activations for global clinical trials

Job Summary

  • The role involves providing administrative and technical support to ensure audit readiness and rapid site activations for global clinical trials.
  • Candidates will manage eTMF reviews, coordinate Investigator Site File materials, and analyze study metrics to maintain high-quality standards.
  • This position requires working the third shift (nights) while collaborating with a global team across over 100 countries.

Matching Summary

The role involves providing administrative and technical support to ensure audit readiness and rapid site activations for global clinical trials.

Skills & Requirements

Must-have

  • eTMF system proficiency
  • site activation critical path
  • ICH GCP knowledge
  • SOP adherence
  • third shift availability

Nice-to-have

  • local language skills
  • new staff training experience
  • strong negotiation skills
  • risk escalation capability

Key Requirements

  • High school diploma or equivalent
  • Bachelor's degree preferred
  • 0 to 1 year relevant experience

Work Rights

Not specified

Tailored Resume

Cover Letter