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Freelance CRA - Czech Republic

IQVIA · Prague, Czechia

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Clinical OperationsPart-timeCompany career page

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Role summary

IQVIA seeks a freelance Clinical Research Associate to support two Phase III oncology trials across Czech Republic sites. The role involves site monitoring, GCP compliance oversight, and data integrity management over approximately five months at 0.5 FTE.

What they're looking for

  • 2+ years CRA experience including site monitoring
  • Oncology or hematology background
  • Proficiency in clinical trial processes and GCP regulations
  • Fluent in Czech and English languages
  • Strong organizational and communication abilities
  • Ability to work independently and prioritize multiple tasks

What you'll be doing

  • Conduct site evaluations, initiations, monitoring visits, and close-outs
  • Ensure GCP compliance and maintain data integrity standards
  • Provide training and support to site staff for issue resolution
  • Review protocols, study manuals, and electronic case report forms
  • Track investigational product inventory and attend investigator meetings

Privacy & handoff

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What RoleLantern checked

This role is listed from an approved source. RoleLantern checks that the application link is live and how recently the role appeared — the employer has not confirmed it directly on RoleLantern.

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RoleLantern checkedNeeds clarity
Date posted7 days ago
Last source checkToday
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