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Clinical Site Associate at ICON plc - ApplyBlast

Clinical Site Associate

ICON plc

4 months ago

Paris, France

Hybrid

Full Time

Junior

0 applicants

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About this role

A Clinical Site Associate at ICON supports clinical trial operations by ensuring site compliance, managing documentation accuracy, and preparing for audits. Based in Paris, this initial office-based role serves as a stepping stone to a traveling Clinical Research Associate position, focusing on site coordination, training, and regulatory adherence.

Responsibilities

Provide clinical site support and oversight
Manage site-level communications in French and English
Coordinate site trainings and systems access
Maintain Trial Master File documentation accuracy
Support readiness activities for audits and inspections

Skills

Qualifications

Bachelor's in Life SciencesMaster's in Healthcare6–18 months clinical research experience

About ICON plc

iconplc.com

Headquarters

South Dublin, Ireland

Company Size

10001+ employees

Founded

1990

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ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.