Clinical Research Associate - South East

Mdcrecruiting

South East England, , GB
Fully remote
Site management and monitoring activities
Compliance with ich-gcp and local regulations
Clinical trial protocol adherence
Our company is committed to advancing high-quality clinical research that upholds ICH/GCP standards and local regulatory requirements

Job Summary

  • Our company is committed to advancing high-quality clinical research that upholds ICH/GCP standards and local regulatory requirements.
  • You will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to protocols and quality standards.
  • We offer a collaborative environment with growth, mentorship, and continuous improvement alongside competitive compensation and benefits.

Matching Summary

Our company is committed to advancing high-quality clinical research that upholds ICH/GCP standards and local regulatory requirements.

Skills & Requirements

Must-have

  • Site management and monitoring activities
  • Compliance with ICH-GCP and local regulations
  • Clinical trial protocol adherence
  • Adverse event reporting system
  • Clinical trials monitoring
  • Strong IT proficiency with clinical applications

Nice-to-have

  • Mentoring and leadership capability
  • Effective communication and interpersonal skills
  • Solution-oriented approach to complex issues
  • Customer-focused mindset
  • Experience conducting site motivation visits
  • Ability to work in multicultural settings

Key Requirements

  • Bachelor’s degree or higher
  • Extensive direct site management experience
  • Valid driver’s license preferred
  • Ability to travel 65–75% domestically and internationally

Work Rights

Not specified

Tailored Resume

Cover Letter