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CRA II - Medical Device

JR065852

About the role

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

This is an exciting opportunity to join ICON

Clinical Research Associate II - Medical Device

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?

We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.

The role

  • Working independently and proactively to coordinate all necessary activities required 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

  • Managing sponsor generated queries efficiently and responsible for study cost effectiveness

  • Dependent on level of experience you may assist in training and mentoring less experienced CRA's and/or manage CRA's working on international projects

What you need

  • Minimum of 18 months of active independent field monitoring experience- all types of visits.

  • Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data

  • Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner

  • Ability to produce accurate work to tight deadlines within a pressurized environment.

  • Medical Device experience.

Why join us?

  • Ongoing development is vital to us, and as a CRA II you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. Our benefits package is competitive, our scope is international and we genuinely care about our people and their success.

Benefits of Working in ICON

Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.

We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.

ICON is an equal opportunity employer, including disability/veteran, and committed to providing a workplace free of discrimination and harassment.

List #1

Day in the life

Lydia's Journey Back to ICON

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Our People

Content type

Blogs

Publish date

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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Driving Trials Forward: Study Start-Up Leadership at ICON

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Our People

Content type

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Publish date

03/16/2026

Summary

Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl

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Explore James Pereira's career in study start-up at ICON, leading global teams to accelerate patient access.

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Who’s Who in a Clinical Trial Team

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Who's Who In a Clinical Trial Team Clinical trials rely on large, cross functional teams working together across countries, time zones and specialisms. For those new to the industry, the number of

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Understand the key roles in a clinical trial team, from study start up and site activation to data, safety and quality.

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