Clinical Trial Coordinator

Mdcrecruiting

Denmark
Onsite
Clinical trial management systems (ctms)
Ich-gcp compliance
Document management and quality control
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, Clinical Research Managers, Clinical Research Associates, 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

  • Clinical Trial Management Systems (CTMS)
  • ICH-GCP compliance
  • Document management and quality control

Nice-to-have

  • Positive mindset and resilience
  • Cross-functional collaboration
  • Continuous improvement mindset

Key Requirements

  • Bachelor’s degree in life sciences or related field
  • Experience in a clinical research environment
  • Fluency in English and Danish

Work Rights

Not specified

Tailored Resume

Cover Letter