Clinical Research Associate - Scotland

29

Scotland, United Kingdom
**
Ich/gcp compliance knowledge
Site management and monitoring
Protocol adherence expertise
** The job posting is for a Clinical Research Associate (CRA) position based in Scotland, which involves significant travel (65-75%) to oversee clinical study protocols and ensure compliance with ICH/GCP standards. The role focuses on building relationships with investigative sites, conducting site management activities, and mentoring junior CRAs. **

Job Summary

  • The role involves leading performance and compliance for assigned protocols and sites while ensuring rigorous adherence to ICH/GCP standards.
  • Candidates will perform remote and on-site monitoring to ensure data integrity, subject safety, and proper adverse event reporting.
  • The position offers opportunities to shape clinical research at high-performing sites within a collaborative environment focused on growth and mentorship.

Matching Summary

Match Score: 75

** The job posting is for a Clinical Research Associate (CRA) position based in Scotland, which involves significant travel (65-75%) to oversee clinical study protocols and ensure compliance with ICH/GCP standards. The role focuses on building relationships with investigative sites, conducting site management activities, and mentoring junior CRAs. **

Skills & Requirements

Must-have

  • ICH/GCP compliance knowledge
  • Site management and monitoring
  • Protocol adherence expertise
  • Adverse event reporting
  • Data integrity assurance
  • Remote and on-site visits

Nice-to-have

  • Mentoring junior CRAs
  • Root cause analysis skills
  • Cross-functional collaboration
  • Process improvement mindset
  • Culturally sensitive relationships

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter