Clinical Research Associate, Sponsor Dedicated

ICON Broadbean

Multiple Locations
Oncology and dermatology experience
Site qualification and monitoring
Protocol compliance and data integrity
As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials

Job Summary

  • As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials.
  • You will ensure protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff will facilitate smooth study conduct.

Matching Summary

As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials.

Skills & Requirements

Must-have

  • Oncology and Dermatology experience
  • Site qualification and monitoring
  • Protocol compliance and data integrity

Nice-to-have

  • Strong organizational skills
  • Ability to work collaboratively
  • Attention to detail

Key Requirements

  • Bachelor's degree in a scientific field
  • Minimum of 2 years as a Clinical Research Associate
  • In-depth knowledge of ICH-GCP guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter