Clinical Research Associate - South East

Memorialdrivevetclinic

South East England, United Kingdom
Fully remote
Ich/gcp standards
Site management and monitoring
Adverse event reporting
Serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations, and company policies

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 reports.
  • Contribute to country strategy by identifying and onboarding potential new sites and mentoring junior CRAs.

Matching Summary

Serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations, and company policies.

Skills & Requirements

Must-have

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

Nice-to-have

  • mentoring junior CRAs
  • drive continuous improvement
  • culturally sensitive relationships
  • customer-focused mindset

Key Requirements

  • Bachelor's degree or higher
  • Extensive direct site management experience
  • Fluent in English
  • Robust knowledge of clinical research regulations

Work Rights

Not specified

Tailored Resume

Cover Letter