Senior Cra

ICON Clinical Research, LP

Portugal
Clinical trial site monitoring
Adherence to study protocols
Regulatory requirements and gcp
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement

Job Summary

  • You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
  • ICON plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment driving innovation and excellence.
  • 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

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Skills & Requirements

Must-have

  • Clinical trial site monitoring
  • Adherence to study protocols
  • Regulatory requirements and GCP
  • Site performance assessment
  • Cross-functional team collaboration
  • Data collection and reporting
  • Site staff training and guidance

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Continuous improvement focus
  • Building effective relationships
  • Influencing and driving compliance

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter