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Clinical Research Associate (CRA 2/Sr CRA 1) - Sponsor dedicated - Hungary

IQVIA · Budapest, Hungary

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Role summary

IQVIA seeks a Clinical Research Associate to monitor clinical trial sites and manage study conduct in Hungary. The role encompasses site visits, protocol oversight, recruitment coordination, and regulatory compliance to ensure adherence to study protocols and regulatory standards.

What they're looking for

  • Bachelor's degree in scientific or healthcare discipline
  • Minimum 1 year of on-site clinical trial monitoring experience
  • Therapeutic and protocol knowledge
  • Fluent in English and Hungarian, written and verbal
  • IT proficiency and strong organizational skills
  • Ability to manage time, finances, and stakeholder relationships
  • Located in Hungary

What you'll be doing

  • Conduct site selection, initiation, monitoring, and close-out visits
  • Develop and track subject recruitment plans aligned with study milestones
  • Administer protocol training and maintain ongoing site communication
  • Monitor protocol compliance, data quality, and regulatory adherence
  • Manage study documentation including TMF, ISF, visit reports, and data queries

Privacy & handoff

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RoleLantern checkedNeeds clarity
Date posted16 days ago
Last source check1 day ago
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