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ICON Clinical Research, LP

United Kingdom
Monitor clinical trial sites
Ensure adherence to protocols
Conduct site visits
As a Senior CRA for the Full-Service team at ICON, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards

Job Summary

  • As a Senior CRA for the Full-Service team at ICON, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

As a Senior CRA for the Full-Service team at ICON, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

Skills & Requirements

Must-have

  • Monitor clinical trial sites
  • Ensure adherence to protocols
  • Conduct site visits
  • Collaborate with cross-functional teams
  • Build effective relationships with site personnel

Nice-to-have

  • Foster an inclusive environment
  • Drive innovation and excellence
  • Nurture talent
  • Focus on well-being and work life balance

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate
  • Proven ability to manage multiple sites
  • Proficiency in relevant clinical trial software
  • Ability to travel domestically 6-8 days per month

Work Rights

Not specified

Tailored Resume

Cover Letter