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Imaging Scientist

JR070829

About the role

This vacancy has now expired. Please click here to view live vacancies.

At ICON, it's our people that set us apart.

As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry! Are you one of them?

At ICON, we have an incredible opportunity for a Imaging Scientist to join the Medical Imaging team in the US or the EU.

The role:

  • Provide scientific oversight for Blinded Independent Central Review (BICR) implementation for clinical trials based on:
    • Study protocol
    • Analysis criteria
    • Regulatory documents
    • Imaging charter
  • Review the following imaging charter documents to ensure alignment to study protocol, read criteria and Standard Operating Procedures:
    • Site Imaging Manual
    • Imaging Review Charter
    • Independent Review Training Manual
    • Image analysis platform configuration
    • Case Report Forms
  • Facilitate and support sponsor meetings related to Imaging Review Charter development and adherence
  • Consult with radiologists, oncologists and other medical professional to support Imaging Review Charter development
  • Provide training support for the BICR
  • Provide support and guidance of development of analysis criteria related checks
  • Provide guidance and support of the User Acceptance Testing of analysis systems and tools
  • Develop training materials for internal training library
  • Support reader performance reports and remediation
  • Analyze developments in read criteria
  • Review and develop Standard Operating Procedures and Work Instruction
  • Review process flows and work with leadership toward quality improvements, as appropriate
List #1

Day in the life

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Leading Through Change: Zhong Yao's Journey at ICON in China

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Content type

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Publish date

12/10/2025

Summary

Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.

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From culture to collaboration, Zhong Yao explains how ICON China delivers quality clinical trials, and empowers local talent.

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How Data Moves Through a Clinical Trial

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Publish date

12/01/2025

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How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i

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Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

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Quality and Compliance - A Plain Language Guide

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Quality and Compliance for New Entrants:           A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job

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A clear, practical introduction to quality and compliance for those starting a career in clinical research.

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