Clinical Research Associate - South East

29

South East England, United Kingdom
Fully remote
Ich/gcp standards
Site management and monitoring
Adverse event reporting
The position of Clinical Research Associate (CRA) at 29 involves leading site management and compliance for clinical studies in South East England, requiring substantial travel (65-75%). The ideal candidate will have extensive experience in clinical research, particularly in monitoring and site management, and will be responsible for ensuring adherence to regulatory standards

Job Summary

  • Serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations, and company policies.
  • Perform site management and monitoring activities, including validation, initiation, monitoring, and close-out visits, documenting clear and comprehensive reports.
  • Contribute to country strategy by identifying and onboarding potential new sites, building site capabilities, and mentoring junior CRAs.

Matching Summary

Match Score: 85

The position of Clinical Research Associate (CRA) at 29 involves leading site management and compliance for clinical studies in South East England, requiring substantial travel (65-75%). The ideal candidate will have extensive experience in clinical research, particularly in monitoring and site management, and will be responsible for ensuring adherence to regulatory standards.

Skills & Requirements

Must-have

  • ICH/GCP standards
  • site management and monitoring
  • adverse event reporting
  • protocol conduct
  • data integrity
  • patient safety

Nice-to-have

  • mentoring junior CRAs
  • culturally sensitive relationships
  • growth-oriented demeanor

Key Requirements

  • Bachelor's degree or higher
  • Extensive direct site management experience
  • Fluent in English
  • Valid driver's license preferred

Work Rights

Not specified

Tailored Resume

Cover Letter