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ICON

Los Angeles, CA, United States
Onsite
Clinical trial monitoring experience
Protocol compliance and data integrity
Site qualification and initiation visits
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.
  • As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • Clinical trial monitoring experience
  • Protocol compliance and data integrity
  • Site qualification and initiation visits
  • Patient safety management
  • Data review and query resolution
  • Travel up to 60% required
  • Valid driver’s license

Nice-to-have

  • Strong organizational skills
  • Effective communication skills
  • Ability to work independently
  • Collaborative team player
  • Attention to detail
  • Fast-paced environment adaptability

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 9 months onsite CRA monitoring experience
  • In-depth knowledge of ICH-GCP guidelines
  • Ability to travel internationally and domestically
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

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