Cra (level Ii)

PPD (Thermo Fisher) UK

Beijing, China
On-site
Risk-based monitoring approach
Ich-gcp guidelines
Site processes specialist
PPD (Thermo Fisher) is seeking a Clinical Research Associate (Level II) to join their team in Beijing, China. The role involves monitoring clinical trials, ensuring compliance with protocols and regulations, and managing documentation, with a focus on building collaborative relationships with investigational sites

Job Summary

  • Perform and coordinate all aspects of the clinical monitoring and site management process, ensuring trial compliance and data reliability.
  • Conduct remote or on-site visits to assess protocol and regulatory compliance, manage documentation, and ensure audit readiness.
  • Develop collaborative relationships with investigational sites and facilitate effective communication between sites, clients, and project teams.

Matching Summary

Match Score: 85

PPD (Thermo Fisher) is seeking a Clinical Research Associate (Level II) to join their team in Beijing, China. The role involves monitoring clinical trials, ensuring compliance with protocols and regulations, and managing documentation, with a focus on building collaborative relationships with investigational sites.

Skills & Requirements

Must-have

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

Nice-to-have

  • Root cause analysis
  • Critical thinking and problem-solving
  • Collaborative relationships with sites
  • Project publications/tools contribution

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter