Cra (level Ii)

Thermo Fisher Scientific UK

Beijing, China
On-site
Risk-based monitoring approach
Ich-gcp guidelines
Site processes specialist
Thermo Fisher Scientific is seeking a Clinical Research Associate (Level II) in Beijing, China, who will be responsible for monitoring clinical trials, ensuring protocol compliance, and managing site relationships. The role requires a strong background in clinical monitoring, critical thinking skills, and a solid understanding of regulatory guidelines

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, the client, and the project team.

Matching Summary

Match Score: 85

Thermo Fisher Scientific is seeking a Clinical Research Associate (Level II) in Beijing, China, who will be responsible for monitoring clinical trials, ensuring protocol compliance, and managing site relationships. The role requires a strong background in clinical monitoring, critical thinking skills, and a solid understanding of regulatory guidelines.

Skills & Requirements

Must-have

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

Nice-to-have

  • Root cause analysis
  • Critical thinking and problem-solving
  • Collaborative relationships with investigational sites
  • Adaptable in a wide range of scenarios

Key Requirements

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

Work Rights

Not specified

Tailored Resume

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