Clinical Research Associate (cra 2/sr Cra 1) - Sponsor Dedicated - Hungary

IQVIA UK

Hungary
**
Perform site monitoring visits
Manage subject recruitment plans
Ensure gcp/ich regulatory adherence
** IQVIA is seeking a Clinical Research Associate (CRA) with at least one year of on-site monitoring experience to manage clinical trial sites in Hungary. The role involves ensuring compliance with study protocols and regulations, facilitating effective communication with site personnel, and managing study progress and documentation. **

Job Summary

  • The role involves performing selection, initiation, monitoring, and close-out visits to ensure sites conduct studies according to the protocol.
  • Candidates must evaluate the quality of site practices and manage regulatory submissions, recruitment progress, and case report form completion.
  • The position requires maintaining the Investigator's Site File in accordance with GCP, ICH, and local regulatory requirements.

Matching Summary

Match Score: 75

** IQVIA is seeking a Clinical Research Associate (CRA) with at least one year of on-site monitoring experience to manage clinical trial sites in Hungary. The role involves ensuring compliance with study protocols and regulations, facilitating effective communication with site personnel, and managing study progress and documentation. **

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Manage subject recruitment plans
  • Ensure GCP/ICH regulatory adherence
  • Maintain Trial Master File documentation
  • Generate and resolve data queries

Nice-to-have

  • Strong problem-solving skills
  • Effective time management abilities
  • Excellent verbal communication in English
  • Collaborative team player mindset

Key Requirements

  • Bachelor's degree in scientific discipline or healthcare
  • 1+ years of on-site monitoring experience
  • Fluency in English and Hungarian languages
  • Located in Hungary

Work Rights

Must be located in Hungary

Tailored Resume

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