Clinical Trial Coordinator

mnssazn.top

Denmark
Onsite
Ich-gcp compliance
Etmf management
Ctms management
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 compliance
  • eTMF management
  • CTMS management
  • document excellence
  • site readiness coordination

Nice-to-have

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

Key Requirements

  • Bachelor's degree preferred
  • Fluent in English and Danish
  • Experience in clinical research environment

Work Rights

Not specified

Tailored Resume

Cover Letter