Cra - Future Roles (france)

Syneos Health

Paris, France
On-site
Ich-gcp and/or gpp compliance
Protocol compliance
Site qualification and initiation
Perform site qualification, initiation, monitoring, management, and close-out visits ensuring regulatory and protocol compliance

Job Summary

  • Perform site qualification, initiation, monitoring, management, and close-out visits ensuring regulatory and protocol compliance.
  • Assess site processes, conduct source document review, verify data accuracy, and drive query resolution to closure.
  • Maintain a working knowledge of GCP guidelines, relevant regulations, and company SOPs while protecting subject confidentiality.

Matching Summary

Perform site qualification, initiation, monitoring, management, and close-out visits ensuring regulatory and protocol compliance.

Skills & Requirements

Must-have

  • ICH-GCP and/or GPP compliance
  • protocol compliance
  • site qualification and initiation
  • monitoring and close-out visits
  • subject safety and data integrity assessment
  • Investigational Product (IP) handling
  • Investigator Site File (ISF) review
  • audit readiness standards

Nice-to-have

  • adapt to changing priorities
  • support subject recruitment
  • Total Self culture
  • diversity of thoughts and backgrounds

Key Requirements

  • Bachelor's degree or RN in a related field
  • Knowledge of Good Clinical Practice/ICH Guidelines
  • Ability to manage required travel of up to 75%

Work Rights

Not specified

Tailored Resume

Cover Letter