Clinical Trial Coordinator

Vetamc

Denmark
Onsite
Ich-gcp compliance
Etmf management
Ctms proficiency
Make a real impact on patients’ lives by powering high-quality, compliant clinical trials across a multi-country cluster

Job Summary

  • Make a real impact on patients’ lives by powering high-quality, compliant clinical trials across a multi-country cluster.
  • Your work ensures site readiness, regulatory compliance (including ICH-GCP), and on-time delivery of trial milestones.
  • We offer a dynamic and international work environment where you will have the opportunity to grow and develop your skills while contributing to meaningful research.

Matching Summary

Make a real impact on patients’ lives by powering high-quality, compliant clinical trials across a multi-country cluster.

Skills & Requirements

Must-have

  • ICH-GCP compliance
  • eTMF management
  • CTMS proficiency
  • document management
  • site readiness coordination
  • regulatory submissions support

Nice-to-have

  • innovative mindset
  • continuous improvement
  • cross-functional collaboration
  • resilient and adaptable
  • analytical problem solving

Key Requirements

  • Bachelor's degree preferred
  • Experience in clinical research
  • Knowledge of ICH-GCP
  • Fluent in English and Danish

Work Rights

Not specified

Tailored Resume

Cover Letter