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Parexel

Clinical Research Associate II – FSP

Parexel

Clinical Research Associate II supporting clinical trials and ensuring compliance with regulations at Parexel. Responsibilities include site monitoring, reporting, and investigator training.

Posted 5/10/2026full-timeRemote • 🇨🇳 ChinaJuniorMid-LevelWebsite

About the role

Key responsibilities & impact
  • Drive study performance at the sites
  • Perform site monitoring and other onsite visit activities
  • Provide the required monitoring visit reports within required timelines
  • Proactively identify study-related issues and escalates to Local Study Teams
  • Train, support and advise Investigators and site staff in study related matters

Requirements

What you’ll need
  • Minimum 2-year experience as CRA
  • Understanding of the clinical dataflow
  • Good knowledge of the clinical study and drug development processes
  • Fluent in both oral and written English
  • Bachelor's degree in biological science or healthcare-related field, or equivalent

Benefits

Comp & perks
  • Health insurance
  • Professional development opportunities
  • Flexible working arrangements

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
clinical dataflowclinical study processesdrug development processes
Soft Skills
communicationtrainingsupportadvisingproblem-solving