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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

Heartbeat vitals on monitor
Central Monitoring vs On Site Monitoring

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Industry

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Blogs

Publish date

04/03/2026

Summary

Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re

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Learn the difference between central monitoring and on site monitoring and how both support patient safety and data quality.

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Francis' Journey back to ICON

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Our People

Content type

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Publish date

03/26/2026

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Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February

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Francis Kayamba shares what drew him back to ICON and how the sponsor-embedded model works.

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Lydia's Journey Back to ICON

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Our People

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03/24/2026

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Career paths are rarely straightforward, especially in the fast moving world of clinical research. For many professionals, gaining experience across organisations can provide valuable perspectiv

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Learn about Lydia's return to ICON and why she felt it was a natural choice.

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