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SMA II

JR063840

About the role

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

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?

As a Site Management Associate at ICON, you'll be responsible for managing, implementing and monitoring clinical studies in a team setting.

The Role

  • Identifying, training/initiating and closing out study sites
  • Conducts and completes remote site management activities, with support as needed, according to the Site Management Plan.
  • Manage study sites and required protocols, amendments and deviations.
  • Assure data is reported accurately and timeline are maintained.
  • Serves as the primary contact for sites and investigates participating in studies.
  • Maintains, reviews, and ensures adequacy of information and data contained in site management reports, tracking systems (CTMS or others) and other site management documents.
  • Review drug storage and drug accountability procedures in accordance with applicable SOPs.

What you need

  • Bachelor's degree or local equivalent in medicine, science or related discipline.
  • Minimum of one year of relevant experience in a health care or research environment strongly preferred.
  • Ability to review and evaluate clinical data
  • Strong oral and written communication skills
  • This position may require travel up to 25% of the time

Why join us?

Ongoing development is vital to us, 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.

ICON Plc is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment.

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.

Apply
List #1

Day in the life

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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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Inside ICON

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Publish date

03/15/2026

Summary

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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Understanding Roles in a Clinical Trial: Sponsors, CROs, and Sites

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What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh

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Learn how clinical trials are delivered by understanding the roles of sponsors, CROs, and sites.

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