Fsp Cra (level Ii)

Thermo Fisher Scientific UK

Guangzhou, China
Fully remote
Risk-based monitoring approach
Ich-gcp guidelines
Site processes specialist
As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation

Job Summary

  • As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
  • You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.).
  • You will ensure audit readiness and develop collaborative relationships with investigational sites.

Matching Summary

As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.

Skills & Requirements

Must-have

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

Nice-to-have

  • Root cause analysis
  • Critical thinking and problem-solving
  • Collaborative relationships
  • Effective communication
  • Adaptable in wide range of scenarios

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter