Senior Cra

ICON plc

Copenhagen, Denmark
Fully remote
Overseeing and managing clinical trial activities
Ensure data integrity, participant safety
Monitoring clinical trial sites
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 plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
  • Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

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

  • overseeing and managing clinical trial activities
  • ensure data integrity, participant safety
  • monitoring clinical trial sites
  • adherence to study protocols
  • GCP standards
  • conducting site visits
  • resolve issues
  • site performance assessment
  • timely and accurate data collection
  • training and guidance to site staff
  • building and maintaining effective relationships

Nice-to-have

  • foster an inclusive environment
  • driving innovation and excellence
  • diverse and dynamic team
  • work life balance opportunities
  • inclusion & belonging are fundamental

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate
  • strong understanding of clinical trial processes
  • Proven ability to manage multiple sites
  • strong organizational and problem-solving skills
  • Expertise in monitoring practices
  • proficiency in relevant clinical trial software
  • Ability to travel at least 60% of the time
  • possess a valid driver's license

Work Rights

Not specified

Tailored Resume

Cover Letter