Centralized Monitor

IQVIA UK

Fully remote
Subject level data review
Remote monitoring visits
Study central monitoring plan
The role involves managing assigned sites and performing independent Subject Level Data Reviews to ensure patient information accuracy

Job Summary

  • The role involves managing assigned sites and performing independent Subject Level Data Reviews to ensure patient information accuracy.
  • Candidates must conduct centralized monitoring activities, analyze site-level risks, and provide actionable insights to improve clinical trial quality.
  • The position requires adherence to ICH GCP guidelines, protocol compliance, and the ability to mentor junior team members.

Matching Summary

The role involves managing assigned sites and performing independent Subject Level Data Reviews to ensure patient information accuracy.

Skills & Requirements

Must-have

  • Subject Level Data Review
  • Remote Monitoring Visits
  • Study Central Monitoring Plan
  • ICH GCP Compliance
  • Clinical Trial Conduct

Nice-to-have

  • Mentorship to Associate Monitors
  • Analytical Inferences Writing
  • Cross-cultural Communication
  • Process Improvement Inputs
  • Technical Solution Specialist Role

Key Requirements

  • Bachelor's degree in clinical or life sciences
  • Minimum 2 years of relevant work experience
  • Advanced knowledge of ICH GCP regulations
  • Experience in clinical research field preferred
  • Strong written and verbal communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter