Sr Cra

ICON Clinical Research, LP

Frankfurt, Germany
Clinical trial monitoring
Site performance assessment
Data collection and reporting
Oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards

Job Summary

  • Oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
  • 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.

Matching Summary

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
  • Site performance assessment
  • Data collection and reporting
  • GCP standards adherence
  • Stakeholder relationship management

Nice-to-have

  • Fostering inclusive environment
  • Driving innovation and excellence
  • Continuous improvement focus
  • Guiding other CRAs

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter