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JR066211

About the role

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

As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.

The Role

  • Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
  • Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
  • Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
  • Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness
  • Dependent on level of experience you may assist in training and mentoring less expert CRA's and/or lead CRA's working on international projects

What you need

  • +1 years of monitoring experience as a CRA
  • Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
  • You will possess excellent written and verbal communication in English
  • Ability to produce accurate work to tight deadlines within a pressurized environment
  • You will be asked to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license
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Day in the life

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Interviewing at ICON

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Inside ICON

Content type

Blogs

Publish date

01/05/2026

Summary

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Learn what to expect when interviewing at ICON, and how hiring decisions are always made by people.

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Content type

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Publish date

01/05/2026

Summary

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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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