Clinical Trial Coordinator

Nerdgigs

Denmark
Onsite
Ich-gcp knowledge
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.
  • You’ll be the central connector for Clinical Operations Managers (COM), Clinical Research Managers (CRM), Clinical Research Associates (CRA), and study sites across multiple countries.
  • 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 knowledge
  • eTMF management
  • CTMS proficiency
  • document management
  • site readiness
  • regulatory compliance

Nice-to-have

  • growth mindset
  • continuous improvement
  • analytical problem solving
  • resilient and adaptable

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter