Cra Ii

ICON

Burlington, Canada
Fully remote
Clinical trial monitoring and site visits
Protocol compliance and patient safety
Data review and query resolution
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

Job Summary

  • 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 range of benefits focused on well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
  • ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to a workplace free of discrimination and harassment.

Matching Summary

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.

Skills & Requirements

Must-have

  • Clinical trial monitoring and site visits
  • Protocol compliance and patient safety
  • Data review and query resolution
  • Collaboration with investigators and site staff
  • Travel up to 60% internationally and domestically

Nice-to-have

  • Strong organizational and communication skills
  • Ability to work independently and collaboratively
  • Attention to detail
  • Inclusive and diverse work environment

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 2 years experience as Clinical Research Associate
  • In-depth knowledge of clinical trial processes and ICH-GCP guidelines
  • Valid driver’s license
  • Ability to travel at least 60%

Work Rights

Not specified

Tailored Resume

Cover Letter