Clinical Research Associate Ii / Senior Clinical Research Associate Biotech

ICON Clinical Research, LP

Frankfurt, Germany
Monitoring clinical trial sites
Adherence to study protocols
Gcp standards
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards

Job Summary

  • As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
  • We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team.
  • Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

Skills & Requirements

Must-have

  • Monitoring clinical trial sites
  • Adherence to study protocols
  • GCP standards
  • Data integrity
  • Participant safety
  • Compliance

Nice-to-have

  • Inclusive environment
  • Drive innovation and excellence
  • Foster a diverse culture
  • Well-being and work life balance

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate
  • Strong understanding of clinical trial processes
  • Proven ability to manage multiple sites
  • Proficiency in relevant clinical trial software
  • Excellent communication skills in German and English

Work Rights

Not specified

Tailored Resume

Cover Letter