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Clinical Trial Associate

ICON · Copenhagen, Denmark

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Clinical OperationsFull-timeCompany career page

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What they're looking for

  • Bachelor's degree in scientific or healthcare-related field
  • Prior experience or demonstrated interest in clinical research
  • Knowledge of clinical trial processes, regulations, and guidelines
  • Strong organizational and written/verbal communication skills
  • Ability to work collaboratively with attention to detail in fast-paced settings
  • Willingness to travel approximately 10% as required
  • Legal right to work in Denmark

What you'll be doing

  • Coordinate and administer clinical trials while ensuring protocol and regulatory compliance
  • Maintain and organize clinical trial documentation, study files, and regulatory submissions
  • Support preparation of study materials including informed consent and case report forms
  • Facilitate communication across cross-functional teams to support trial execution
  • Track and report clinical trial metrics and key milestones

Privacy & handoff

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What RoleLantern checked

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