Experienced Cra 1; Southeast Location

PPD (Thermo Fisher) UK

Southeast, UK
Remote
Risk-based monitoring approach
Ich-gcp guidelines
Regulatory compliance
PPD (Thermo Fisher) is seeking an Experienced Clinical Research Associate I to support clinical trials in the Southeast UK. The role involves monitoring investigator sites, ensuring regulatory compliance, and maintaining strong communication with various 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

PPD (Thermo Fisher) is seeking an Experienced Clinical Research Associate I to support clinical trials in the Southeast UK. The role involves monitoring investigator sites, ensuring regulatory compliance, and maintaining strong communication with various stakeholders.

Skills & Requirements

Must-have

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

Nice-to-have

  • Root cause analysis
  • Critical thinking
  • Problem-solving skills
  • Collaborative relationships
  • Audit readiness

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter