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CRA

  1. Netherlands
2025-117057
  1. Clinical Monitoring
  2. ICON Strategic Solutions (FSP)

About the role

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

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

 

As a senior CRA based in the Netherlands (the Hague area) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently but always as part of the client and ICON plc team.

 


  • Identify, select, initiate and close-out of the study sites for clinical trials
  • Study monitoring to ensure protocol compliance
  • Reply and resolve queries that are being identified during the monitoring visits
  • Reporting of safety issues
  • Writing of monitoring reports and planning the next visits

You are:

 

By preference you hold a Master degree in biomedical sciences or a bachelor in a paramedical field. 

  • 2 years + experience in the CRA role
  • Communicative skills in Dutch and English
  • Heart for clinical research and for your assigned studies/sites
  • You love to communicate with different stakeholder and love to encourage people, drive them and being the point of contact for your studies

Why ICON?

 

Homebased contract with the option to come to the clients' office

  • Varied job with endless developing opportunities and training
  • Dedicated line manager as of the first day!
  • Flexibility work-life
  • Competitive salary package with company car

 

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best-in-class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

 

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Day in the life

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Suzaita's story - an insight into working in Clinical Research

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A Day In The Life

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Blogs

Publish date

04/05/2023

Summary

Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfil

Teaser label

Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

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Suzaita Hipolito

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Suzaita Hipolito

Suzaita Hipolito

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