Sr Cra

ICON Broadbean

Frankfurt, Germany
Clinical trial monitoring
Gcp standards adherence
Site performance assessment
As a Senior CRA at ICON Plc, you will oversee and manage 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 oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
  • You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities.

Matching Summary

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

Skills & Requirements

Must-have

  • Clinical trial monitoring
  • GCP standards adherence
  • Site performance assessment
  • Cross-functional team collaboration
  • Data collection and reporting
  • Site staff training

Nice-to-have

  • Foster inclusive environment
  • Drive innovation and excellence
  • Shape future of clinical development
  • Continuous improvement focus
  • Build stakeholder relationships

Key Requirements

  • Bachelor's degree in relevant discipline
  • Extensive CRA experience
  • Manage multiple sites and projects
  • Proficiency in clinical trial software
  • Willingness to travel 60%

Work Rights

Not specified

Tailored Resume

Cover Letter