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SMA I - 6 month internship, entry level

JR063654

About the role

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Site Management Associate I - 6 month internship, entry level

Office based in Nanterre, Paris

ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work with top pharmaceutical organizations on emerging therapeutic areas including Oncology, Vaccines, CNS, Cardiovascular, and Pain. We are presently in over 40 countries with over 80 offices worldwide and over 10K employees globally. We are comprised of 6 divisions and offer a full-service portfolio of solutions to our clients.

The Site Management Associate is responsible for managing, implementing and monitoring clinical studies within ICO (our late phase division), with support, in a team setting according to ICON SOPs, SSPs and all applicable rules and regulations.

The responsibilities of this position include, but are not limited to:

  • Identifying, training/initiating and closing out study sites.
  • Conducting remote site monitoring visits and/or targeted on-site visits as needed.
  • Conducting remote site management activities.
  • Managing study sites and the required protocols, amendments and/or deviations, assuring that data is reported accurately and timelines are maintained.

A Bachelor's degree in the life sciences, expertise with regulatory guidelines and clinical terminology, and demonstrable strong site management experience will ensure your success on our team.

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Central Monitoring vs On Site Monitoring

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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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Publish date

03/26/2026

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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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Lydia's Journey Back to ICON

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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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