Clinical Research Associate - South East

539

South East England, United Kingdom
Fully remote
Ich/gcp standards
Site management and monitoring
Protocol conduct
This job posting seeks a Clinical Research Associate (CRA) for a position based in South East England, requiring significant travel (65–75%) for site management and monitoring tasks. The ideal candidate should possess robust knowledge of clinical research practices and the ability to mentor junior staff while ensuring compliance with 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, to ensure data integrity and subject protection.
  • Contribute to country strategy by identifying and onboarding potential new sites and building site capabilities.

Matching Summary

Match Score: 85

This job posting seeks a Clinical Research Associate (CRA) for a position based in South East England, requiring significant travel (65–75%) for site management and monitoring tasks. The ideal candidate should possess robust knowledge of clinical research practices and the ability to mentor junior staff while ensuring compliance with regulatory standards.

Skills & Requirements

Must-have

  • ICH/GCP standards
  • site management and monitoring
  • protocol conduct
  • adverse event reporting
  • regulatory documentation review
  • CTMS and eTMF systems

Nice-to-have

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

Key Requirements

  • Bachelor's degree or higher
  • Extensive direct site management experience
  • Fluent in English

Work Rights

Not specified

Tailored Resume

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