Clinical Research Associate - South East

Vetamc

South East England
Fully remote
Experience in clinical research monitoring
Strong knowledge of ich/gcp standards
Ability to travel 65-75% of working time
The company is committed to advancing high-quality clinical research with patient safety at the core

Job Summary

  • The company is committed to advancing high-quality clinical research with patient safety at the core.
  • The role involves leading performance and compliance for clinical study protocols and sites.
  • Employees benefit from a collaborative environment with opportunities for growth and mentorship.

Matching Summary

The company is committed to advancing high-quality clinical research with patient safety at the core.

Skills & Requirements

Must-have

  • Experience in clinical research monitoring
  • Strong knowledge of ICH/GCP standards
  • Ability to travel 65-75% of working time

Nice-to-have

  • Mentoring and leadership skills
  • Customer-focused mindset
  • Solution-oriented approach

Key Requirements

  • Bachelor's degree in relevant field
  • Extensive direct site management experience
  • Fluency in English with strong communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter