Experienced Clinical Research Associate, 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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