Cra Standard

ICON plc

Beijing, China
Not specified (assumed office-based given the location).
Conduct site qualification, initiation, monitoring, close-out visits
Ensure protocol compliance, data integrity, patient safety
Collaborate with investigators and site staff
ICON plc is seeking a Clinical Research Associate II for their Beijing office, emphasizing an inclusive culture and a mission to innovate in clinical development. The role involves conducting various site visits and ensuring compliance and data integrity in clinical trials, requiring a bachelor's degree and at least two years of relevant experience

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.
  • In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

Match Score: 85

ICON plc is seeking a Clinical Research Associate II for their Beijing office, emphasizing an inclusive culture and a mission to innovate in clinical development. The role involves conducting various site visits and ensuring compliance and data integrity in clinical trials, requiring a bachelor's degree and at least two years of relevant experience.

Skills & Requirements

Must-have

  • Conduct site qualification, initiation, monitoring, close-out visits
  • Ensure protocol compliance, data integrity, patient safety
  • Collaborate with investigators and site staff
  • Perform data review and query resolution
  • Prepare and review study documentation

Nice-to-have

  • Foster an inclusive environment
  • Drive innovation and excellence
  • Contribute to advancement of treatments
  • Nurture talent and reward high performance

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 2 years experience as CRA
  • In-depth knowledge of clinical trial processes
  • Knowledge of regulations and ICH-GCP guidelines
  • Ability to travel at least 60% of the time
  • Possess a valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter