Clinical Research Associate Ii (fsp)-cart-郑州

Parexel

Zhengzhou, China
Onsite
Minimum 2-year cra experience
Fluent english and host country language
Knowledge of ich-gcp guidelines
The role involves driving study performance at sites through comprehensive monitoring and adherence to procedural documents

Job Summary

  • The role involves driving study performance at sites through comprehensive monitoring and adherence to procedural documents.
  • Candidates must ensure accurate reporting of Serious Adverse Events and maintain essential documentation compliant with ICH-GCP.
  • Parexel seeks professionals who share a deep conviction in improving global health through clinical development solutions.

Matching Summary

The role involves driving study performance at sites through comprehensive monitoring and adherence to procedural documents.

Skills & Requirements

Must-have

  • Minimum 2-year CRA experience
  • Fluent English and host country language
  • Knowledge of ICH-GCP guidelines
  • Source data verification skills
  • Microsoft software proficiency

Nice-to-have

  • Strong interpersonal collaboration skills
  • Proactive issue identification abilities
  • Experience with audit preparation
  • Empathy in patient-focused work

Key Requirements

  • Bachelor's degree in biological science or healthcare-related field
  • Minimum 2 years of CRA experience
  • Fluency in English and local Chinese language

Work Rights

Not specified

Tailored Resume

Cover Letter