Cra Ii

ICON

Beijing, China
Clinical trial monitoring and management
Protocol compliance and data integrity
Collaborating with clinical site staff
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 competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

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 and management
  • protocol compliance and data integrity
  • collaborating with clinical site staff
  • travel up to 60% internationally and domestically
  • valid driver’s license required

Nice-to-have

  • strong organizational and communication skills
  • ability to work independently and collaboratively
  • attention to detail
  • inclusive and diverse work culture

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter