Cra I - Fsp - France

Thermo Fisher Scientific UK

Remote
Fully remote
Clinical monitoring experience
Knowledge of ich-gcp guidelines
Ability to conduct remote monitoring
As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance

Job Summary

  • As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance.
  • You will ensure audit readiness and develop collaborative relationships with investigational sites.
  • Contributes to other project work and initiatives for process improvement, as required.

Matching Summary

As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance.

Skills & Requirements

Must-have

  • Clinical monitoring experience
  • Knowledge of ICH-GCP guidelines
  • Ability to conduct remote monitoring

Nice-to-have

  • Good interpersonal skills
  • Critical thinking and problem-solving
  • Ability to work independently

Key Requirements

  • Bachelor's degree in life sciences
  • Minimal clinical monitoring experience
  • Valid driver's license where applicable

Work Rights

Not specified

Tailored Resume

Cover Letter