Clinical Research Associate, Sponsor Dedicated

ICON plc

US
Clinical trial monitoring activities
Protocol compliance and patient safety
Site qualification and initiation visits
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies

Job Summary

  • As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
  • Key responsibilities include conducting site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring protocol compliance, data integrity, and patient safety.
  • ICON offers a competitive salary, a range of additional benefits focused on well-being and work-life balance, and fosters an inclusive and accessible environment for all candidates.

Matching Summary

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • Clinical trial monitoring activities
  • Protocol compliance and patient safety
  • Site qualification and initiation visits
  • Data review and query resolution
  • ICH-GCP guidelines knowledge

Nice-to-have

  • Collaborative work environment
  • Innovation and excellence focus
  • Advancement of treatments and therapies

Key Requirements

  • Minimum 2 years CRA experience
  • Bachelor's degree scientific/healthcare
  • Willingness to travel 60%

Work Rights

Not specified

Tailored Resume

Cover Letter