Sr. Clinical Research Associate (Poland)

Added
20 days ago
Type
Full time
Salary
Salary not provided

Related skills

travel gcp project management regulatory filings site monitoring
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๐Ÿ“‹ Description

  • Manage clinical site monitoring for one or more projects.
  • Lead CRA role; coordinate monitoring activities.
  • Recruit and setup study sites; ensure materials delivery.
  • Act as primary site contact; resolve site/patient issues.
  • Collaborate with sponsors and study teams; maintain data.
  • Travel ~5โ€“8+ days per month as needed.

๐ŸŽฏ Requirements

  • College diploma/degree with 4-6 years of CRA experience.
  • Strong communication and collaboration skills.
  • Attention to detail; critical thinking.
  • Ability to travel regularly.
  • Fluency in English required.
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