Clinical Research Associate Ii / Senior Cra - 0.8 Fte

ICON Clinical Research, LP

Oversee and manage clinical trial activities
Ensure data integrity and participant safety
Conduct site visits and provide support
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.
  • You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
  • 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.

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

  • Oversee and manage clinical trial activities
  • Ensure data integrity and participant safety
  • Conduct site visits and provide support
  • Collaborate with cross-functional teams
  • Build and maintain stakeholder relationships

Nice-to-have

  • Foster an inclusive environment
  • Drive innovation and excellence
  • Nurture talent and reward high performance

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 clinical trial software
  • Ability to travel at least 60% of the time
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter