Cra (level Ii)

PPD (Thermo Fisher) UK

Guangdong, China
On-site
Risk-based monitoring approach
Ich-gcp guidelines
Site processes specialist
PPD, a leader in clinical research, is seeking a Clinical Research Associate (Level II) to coordinate clinical monitoring and site management processes in Guangdong, China. The ideal candidate will perform compliance assessments, manage documentation, and foster relationships with investigational sites while ensuring adherence to regulations

Job Summary

  • Perform and coordinate all aspects of the clinical monitoring and site management process, including remote or on-site visits to assess protocol and regulatory compliance.
  • Ensure trial conduct aligns with approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subject rights, well-being, and data reliability.
  • Maintain regular contact with investigative sites to confirm protocol adherence, issue resolution, and timely data recording, while ensuring audit readiness.

Matching Summary

Match Score: 85

PPD, a leader in clinical research, is seeking a Clinical Research Associate (Level II) to coordinate clinical monitoring and site management processes in Guangdong, China. The ideal candidate will perform compliance assessments, manage documentation, and foster relationships with investigational sites while ensuring adherence to regulations.

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP guidelines
  • Site processes specialist
  • Data accuracy review
  • Investigational product assessment

Nice-to-have

  • Root cause analysis
  • Critical thinking and problem-solving
  • Collaborative relationships with sites
  • Effective communication skills

Key Requirements

  • Bachelor's degree in life sciences or RN certification
  • 1 year clinical research monitor experience
  • Valid driver's license

Work Rights

Not specified

Tailored Resume

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