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Sr. Clinical Trial Manager - CV/Transplant/Renal Disease

JR065967

About the role

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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 an expert Clinical Trial Manager to join the Cardiovascular team in the US.

The Role:

The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study. The CTM oversees the clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrolment and study start-up activities, reviews trip reports, implements corrective and preventative action plans, liaises with the Sponsor, vendors & cross-functional teams, identifies & mitigates risks that may impact clinical delivery, and provides reporting & metrics on all clinical activities. The CTM will also participate in Sponsor, Investigator and bid defense meetings.

What you need:

  • 4 year degree or equivalent combination of education & experience
  • Demonstrated ability to drive the clinical deliverables of a study
  • Subject matter expertise in Cardiovascular, Metabolism, Renal or Kidney Disease or Transplant
  • Prior monitoring experience is preferred
  • Ability to travel up to 20%
  • Fluent in local language - both written & verbal
List #1

Day in the life

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25 Years in Clinical Operations at ICON: Ricardo Cortizo Justo Q&A

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Our People

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Publish date

04/08/2026

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Ricardo Cortizo Justo, Director of Clinical Operations and Site Head for Paris at ICON plc, recently marked an exceptional milestone of 25 years with the organisation. Over the course of his career, R

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Ricardo shares insights from 25 years at ICON, covering clinical operations, leadership, and career development.

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Central Monitoring vs On Site Monitoring

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Industry

Content type

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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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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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