Clinical Research Associate I/II

Posted 13hrs ago

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Job Description

Clinical Research Associate implementing and monitoring clinical trials for Parexel in China. Ensuring compliance with regulatory requirements and effective communication with investigative sites.

Responsibilities:

  • Implement and monitor clinical trials
  • Review and verify trial data accuracy
  • Communicate with investigative sites
  • Complete monitoring activity documents
  • Facilitate audits and audit resolution

Requirements:

  • 1+ years of clinical research experience
  • Knowledge of ICH GCP guidelines
  • Proficiency in monitoring and site management
  • Ability to communicate effectively with investigators
  • Must be fluent in English.

Benefits:

  • Professional development opportunities
  • Health insurance