Clinical Research Associate - South East

med-in.at

South East England
Not specified; competitive compensation + benefits...
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 must be prepared to travel domestically and internationally approximately 65–75% of working time to conduct remote and on-site monitoring activities.
  • The position offers a collaborative environment with opportunities for growth, mentorship, and continuous improvement in high-performing clinical research settings.

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; Competitive compensation and benefits offered

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
  • patient recruitment experience
  • solution-oriented 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