Clinical Research Associate

ICON Clinical Research, LP

Australia
Fully remote
Site qualification and monitoring
Protocol compliance and data integrity
Patient safety assurance
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

Job Summary

  • 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 plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment driving innovation and excellence.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities.

Matching Summary

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.

Skills & Requirements

Must-have

  • Site qualification and monitoring
  • Protocol compliance and data integrity
  • Patient safety assurance
  • Collaboration with investigators
  • Data review and query resolution
  • Study documentation preparation

Nice-to-have

  • Inclusive and diverse culture
  • Focus on well-being and work-life balance
  • Innovation and excellence driven

Key Requirements

  • Minimum 2 years independent monitoring experience
  • Bachelor's degree in scientific/healthcare field
  • In-depth knowledge of clinical trial regulations
  • Ability to work independently and collaboratively
  • Valid driver's license

Work Rights

Not specified

Tailored Resume

Cover Letter