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Manager Study Start Up

JR063180

About the role

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

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?

As a Manager Study Start up at ICON, you'll work with coordination, execution, control and completion of Clinical Operations. Ensure delivery and development of the Study Start Up team against key metrics. Work with Leadership to develop and grow capabilities, productivity, and quality. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.

The role

  • Provide direction and accountability for the operational Study Start Up teams and their delivery at regional and site level.
  • Resourcing, line management, training, functional delivery and input on discussions around quality and operational delivery measurements within the Clinical Operations group
  • Conduct regular discussions with direct reports and lead team meetings at regional and manager team level.
  • Assist with training for SSU Managers and Associates as required.
  • Contact for region in regard to operational questions and escalations.
  • Work with Director/Senior Director and/or VP Clinical Operations to communicate all critical issues, business growth opportunities, developing key relationships as well as providing input regarding budgeting discussions to drive productivity and quality within the region.
  • Drive overall delivery at site and regional level, through your operational team to drive execution of service, client satisfaction, quality and efficiencies.
  • Represent Clinical Operations at Sponsor and internal audits.

What you need

  • Bachelor's degree
  • Minimum 6 years Study start Up, Clinical Research experience that includes a minimum 4 years relevant experience as a SSUA, Senior CRA or Principal CRA (in a Lead CRA role), or at least 2 years as a Project Manager, CRA/SSU Manager or equivalent job role. Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
  • Excellent management skills, developed with a collaborative approach to driving performance and success in a global environment
  • Direct experience managing SSUA's / Clinical Research Associates is preferred
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

Content type

Blogs

Publish date

04/08/2026

Summary

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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Our People

Content type

Blogs

Publish date

03/26/2026

Summary

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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