Experienced Bilingual Clinical Research Associate (cra Ii / Senior Cra) - Montreal, Qc

Thermo Fisher Scientific UK

Montreal, QC, Canada
Fully remote
Risk-based monitoring approach
Ich-gcp guidelines
Site processes specialist
Perform and coordinate all aspects of the clinical monitoring and site management process

Job Summary

  • Perform and coordinate all aspects of the clinical monitoring and site management process.
  • Conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
  • Ensure audit readiness and develop collaborative relationships with investigational sites.

Matching Summary

Perform and coordinate all aspects of the clinical monitoring and site management process.

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP guidelines
  • Site processes specialist
  • Remote and on-site visits
  • Root cause analysis

Nice-to-have

  • Collaborative relationships
  • Customer focus
  • Flexibility and adaptability

Key Requirements

  • Bachelor's degree in life sciences or equivalent
  • 1 year clinical research monitor experience
  • Bilingual in French and English

Work Rights

Not specified

Tailored Resume

Cover Letter