Sr Cra/ Clinical Site Manager Ii- Uk

ICON

United Kingdom
Clinical trial monitoring
Site performance assessment
Data integrity assurance
As a Senior CRA at ICON Plc, 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 at ICON Plc, 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.
  • 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 at ICON Plc, 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

  • Clinical trial monitoring
  • Site performance assessment
  • Data integrity assurance
  • Participant safety oversight
  • GCP compliance

Nice-to-have

  • Cross-functional team collaboration
  • Stakeholder relationship management
  • Inclusive and diverse culture
  • Talent nurturing

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate
  • Proven ability to manage multiple sites and projects
  • Proficiency in clinical trial software and tools
  • Ability to travel at least 60% of the time
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter