Senior Cra

ICON Clinical Research, LP

Wisconsin, USA
On-site
Clinical trial monitoring
Gcp standards adherence
Site performance assessment
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
  • GCP standards adherence
  • Site performance assessment
  • Data integrity and site management
  • Stakeholder relationship management

Nice-to-have

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

Key Requirements

  • Bachelor's degree in a relevant scientific or healthcare field
  • Extensive experience as a Clinical Research Associate
  • Proven ability to manage multiple sites
  • Proficiency in relevant clinical trial software
  • Willingness to travel approximately 60%

Work Rights

Not specified

Tailored Resume

Cover Letter