Cra Ii - Hungary

ICON Clinical Research, LP

Hungary
Not specified; not specified; competitive benefits...
Fully remote
Bachelor's degree in scientific field
2 years clinical research associate experience
Knowledge of ich-gcp guidelines
ICON Clinical Research is seeking a Clinical Research Associate II (CRA II) for a fully remote position in Hungary, focusing on clinical trial monitoring and data analysis. The ideal candidate will have a background in clinical trials, particularly in oncology, and possess strong organizational and communication skills

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development.
  • The role involves conducting site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance and patient safety.
  • Candidates will benefit from competitive salary, various annual leave entitlements, health insurance offerings, and a global Employee Assistance Programme.

Matching Summary

Match Score: 85

ICON Clinical Research is seeking a Clinical Research Associate II (CRA II) for a fully remote position in Hungary, focusing on clinical trial monitoring and data analysis. The ideal candidate will have a background in clinical trials, particularly in oncology, and possess strong organizational and communication skills.

Salary

Not specified; Not specified; Competitive benefits including health insurance and retirement planning

Skills & Requirements

Must-have

  • Bachelor's degree in scientific field
  • 2 years clinical research associate experience
  • Knowledge of ICH-GCP guidelines
  • Site qualification and monitoring visits
  • Data review and query resolution

Nice-to-have

  • Oncology experience is an advantage
  • Strong organizational and communication skills
  • Ability to work independently in fast-paced environment
  • Collaborative team player

Key Requirements

  • Minimum 2 years CRA experience
  • Bachelor's degree in science or healthcare
  • In-depth knowledge of clinical trial regulations
  • Willingness to travel approximately 60%

Work Rights

Not specified

Tailored Resume

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