Senior Cra

ICON plc

Portugal
Clinical trial site 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 site monitoring
  • GCP standards adherence
  • Site performance assessment
  • Cross-functional team collaboration
  • Clinical trial software proficiency

Nice-to-have

  • Fostering inclusive environment
  • Driving innovation and excellence
  • Continuous improvement focus

Key Requirements

  • Bachelor's degree in relevant discipline
  • Extensive Clinical Research Associate experience
  • Proven ability to manage multiple sites
  • Willingness to travel approximately 60%

Work Rights

Not specified

Tailored Resume

Cover Letter