Clinical Research Associate (cra) - All Levels

Thermo Fisher Scientific UK

Remote, Türkiye
Fully remote
Ich-gcp guidelines
Site management process
Protocol compliance
Perform and coordinate different aspects of the clinical monitoring and site management process, conducting remote or on-site visits to assess protocol and regulatory compliance

Job Summary

  • Perform and coordinate different aspects of the clinical monitoring and site management process, conducting remote or on-site visits to assess protocol and regulatory compliance.
  • Monitor investigator sites with a risk-based monitoring approach, applying root cause analysis and critical thinking to identify site processes failures and corrective/preventive actions.
  • Thermo Fisher Scientific offers a competitive salary, an extensive benefits package, a flexible working culture, and an award-winning learning and development program.

Matching Summary

Perform and coordinate different aspects of the clinical monitoring and site management process, conducting remote or on-site visits to assess protocol and regulatory compliance.

Skills & Requirements

Must-have

  • ICH-GCP guidelines
  • site management process
  • protocol compliance
  • data accuracy
  • risk-based monitoring

Nice-to-have

  • collaborative relationships
  • award-winning learning and development
  • flexible working culture
  • work-life balance

Key Requirements

  • Bachelor's degree in life science
  • 2+ years independent on-site monitoring experience
  • Proven understanding of ICH-GCP, EU and FDA requirements
  • Fluent in English and Turkish
  • Must be based in Türkiye

Work Rights

Must be based in Türkiye

Tailored Resume

Cover Letter