Clinical Research Associate - South East

Merck & Co., Inc.

South East England, United Kingdom
Not specified; not specified; competitive compensa...
Fully remote
Ich/gcp regulatory knowledge
Site management and monitoring
Adverse event reporting
The role requires leading performance and compliance for assigned protocols and sites within the South East region while ensuring rigorous adherence to ICH/GCP standards

Job Summary

  • The role requires leading performance and compliance for assigned protocols and sites within the South East region while ensuring rigorous adherence to ICH/GCP standards.
  • Candidates will perform remote and on-site monitoring to ensure data integrity, protect subject rights, and execute validation, initiation, and close-out visits.
  • The position offers a collaborative environment with opportunities for growth, mentorship of junior staff, and contribution to global development programs.

Matching Summary

The role requires leading performance and compliance for assigned protocols and sites within the South East region while ensuring rigorous adherence to ICH/GCP standards.

Salary

Not specified; Not specified; Competitive compensation and benefits

Skills & Requirements

Must-have

  • ICH/GCP regulatory knowledge
  • Site management and monitoring
  • Adverse event reporting
  • Protocol adherence expertise
  • 65-75% travel requirement

Nice-to-have

  • Mentoring junior CRAs
  • Root cause analysis skills
  • Cross-functional collaboration
  • Strong written communication
  • Process improvement mindset

Key Requirements

  • Bachelor's degree required
  • Extensive direct site management experience
  • Valid driver's license preferred

Work Rights

Not specified

Tailored Resume

Cover Letter