Sr Central Monitor

ICON

United Kingdom
Review monitoring visit reports
Ensure regulatory compliance
Data quality oversight
As a Senior Central Monitor at ICON, you will play a pivotal role in ensuring the quality and integrity of clinical trial data through comprehensive monitoring and oversight

Job Summary

  • As a Senior Central Monitor at ICON, you will play a pivotal role in ensuring the quality and integrity of clinical trial data through comprehensive monitoring and oversight.
  • ICON offers a diverse culture that rewards high performance and nurtures talent with competitive benefits focused on well-being and work-life balance.
  • ICON is committed to providing an inclusive and accessible environment for all candidates and a workplace free of discrimination and harassment.

Matching Summary

As a Senior Central Monitor at ICON, you will play a pivotal role in ensuring the quality and integrity of clinical trial data through comprehensive monitoring and oversight.

Skills & Requirements

Must-have

  • Review Monitoring Visit Reports
  • Ensure regulatory compliance
  • Data quality oversight
  • Provide feedback to CRAs
  • Escalate concerns to CTM

Nice-to-have

  • Leadership skills
  • Cross-functional collaboration
  • Proficiency in monitoring tools
  • Excellent communication skills
  • Data management and analysis

Key Requirements

  • Advanced degree in life sciences or clinical research
  • At least 1 year experience reviewing Monitoring Visit Reports
  • Experience in clinical monitoring
  • Regulatory compliance knowledge

Work Rights

Must be based in the UK

Sponsorship: available

Tailored Resume

Cover Letter