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ICON

Regional Norway, Norway
Clinical trial monitoring
Protocol compliance
Data integrity management
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
  • As a Clinical Research Associate II 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 a competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and a global employee assistance program.

Matching Summary

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

Skills & Requirements

Must-have

  • clinical trial monitoring
  • protocol compliance
  • data integrity management
  • patient safety assurance
  • clinical study documentation
  • travel at least 60% of time
  • 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 2 years Clinical Research Associate experience
  • In-depth knowledge of clinical trial processes and ICH-GCP guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter