Cra

ICON

Multiple Locations
Clinical trial site monitoring
Good clinical practice (gcp) standards
Data integrity and site management
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 the company is committed to providing a workplace free of discrimination and harassment.

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

  • Clinical trial site monitoring
  • Good Clinical Practice (GCP) standards
  • Data integrity and site management
  • Cross-functional team collaboration
  • Domestic travel across the UK

Nice-to-have

  • Strong organizational skills
  • Problem-solving abilities
  • Excellent communication skills
  • Stakeholder management
  • Training and guidance provision

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive CRA experience
  • Proficiency in clinical trial software and tools
  • Ability to travel domestically in the UK 6-8 days per month

Work Rights

Not specified

Tailored Resume

Cover Letter