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Experienced Clinical Research Associate (CRA) / Senior CRA, Ukraine

IQVIA · Kyiv, Ukraine

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Clinical OperationsFull-timeCompany career page

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Role summary

IQVIA seeks an experienced Clinical Research Associate to conduct site selection, monitoring, and close-out activities for clinical trials in Kyiv. The role involves managing study progress, ensuring regulatory compliance, and collaborating with site teams and clients.

What they're looking for

  • University degree in scientific discipline or healthcare field
  • 2-3 years of on-site clinical trial monitoring experience
  • Proficient in MS Office and general computer applications
  • Fluent in Ukrainian and English languages
  • Strong organizational, time management, and problem-solving abilities
  • Valid class B driver's license
  • Willingness to travel as needed

What you'll be doing

  • Conduct site selection, initiation, monitoring, and close-out visits
  • Support development of subject recruitment strategies and plans
  • Assess site compliance with Good Clinical Practice and ICH guidelines
  • Track regulatory submissions, enrollment progress, and data query resolution
  • Collaborate with site personnel and client representatives on study operations

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What RoleLantern checked

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Date posted2 days ago
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