Senior Cra

ICON plc

Wisconsin, US
On-site
Clinical trial monitoring
Gcp standards adherence
Site performance assessment
ICON plc is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities in Wisconsin, ensuring adherence to protocols and regulatory requirements. The role involves monitoring clinical trial sites, managing multiple projects, and providing guidance to site staff, with an emphasis on quality and continuous improvement

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

Match Score: 85

ICON plc is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities in Wisconsin, ensuring adherence to protocols and regulatory requirements. The role involves monitoring clinical trial sites, managing multiple projects, and providing guidance to site staff, with an emphasis on quality and continuous improvement.

Skills & Requirements

Must-have

  • Clinical trial monitoring
  • GCP standards adherence
  • Site performance assessment
  • Cross-functional team collaboration
  • Stakeholder relationship management

Nice-to-have

  • Quality and continuous improvement focus
  • Independent work and guidance provision

Key Requirements

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

Work Rights

Not specified

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