Fsp Cra (level I)

Thermo Fisher Scientific UK

Shanghai, China
On-site
Risk-based monitoring approach
Ich-gcp guidelines
Data accuracy through sdr, sdv and crf review
Thermo Fisher Scientific UK is seeking a Clinical Research Associate I to join their team in Shanghai, China. The role involves monitoring clinical trials, ensuring compliance with protocols and regulations, and facilitating communication between stakeholders

Job Summary

  • As a Clinical Research Associate I, 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

Match Score: 85

Thermo Fisher Scientific UK is seeking a Clinical Research Associate I to join their team in Shanghai, China. The role involves monitoring clinical trials, ensuring compliance with protocols and regulations, and facilitating communication between stakeholders.

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP guidelines
  • Data accuracy through SDR, SDV and CRF review
  • Investigational product assessment
  • Audit readiness
  • Site processes specialist

Nice-to-have

  • Root cause analysis skills
  • Problem-solving skills
  • Collaborative relationships with sites
  • Assist in preparation of project publications/tools

Key Requirements

  • Bachelor's degree in life sciences or equivalent
  • Minimal clinical monitoring experience (comparable to 2 years)
  • Valid driver's license where applicable

Work Rights

Not specified

Tailored Resume

Cover Letter