Clinical Research Associate Ii

ICON Clinical Research, LP

Zhengzhou, China
On-site
Clinical trial monitoring experience
Knowledge of ich-gcp guidelines
Strong organizational and communication skills
ICON plc is a world-leading healthcare intelligence and clinical research organization

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization.
  • As a CRA II at ICON, you will design and analyze clinical trials, contributing to innovative treatments.
  • ICON offers a range of competitive benefits focused on well-being and work-life balance.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization.

Skills & Requirements

Must-have

  • Clinical trial monitoring experience
  • Knowledge of ICH-GCP guidelines
  • Strong organizational and communication skills
  • Ability to work independently and collaboratively
  • Willingness to travel approximately 60%

Nice-to-have

  • Attention to detail
  • Experience with data review
  • Collaborative team player

Key Requirements

  • Bachelor's degree in a scientific field
  • Minimum of 2 years as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes

Work Rights

Not specified

Tailored Resume

Cover Letter