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Clinical Study Coordinator at ICON plc - ApplyBlast

Clinical Study Coordinator

ICON plc

4 months ago

Netherlands

Onsite

Full Time

Senior

0 applicants

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About this role

A Clinical Study Coordinator at ICON prepares, coordinates, and executes clinical studies with a focus on high-quality documentation, communication, and protocol adherence. The role involves collaborating with site study teams to ensure timely delivery, managing study materials, and supporting protocol evaluations in a global healthcare research environment.

Responsibilities

Assess, prepare, and execute clinical studies for timely delivery
Coordinate and oversee clinical study execution while ensuring protocol compliance
Prepare clinical study documents for submission to ethical review boards
Support evaluation of protocols, budgets, and case report forms
Develop study-specific instructions and identify staff training needs

Skills

Qualifications

Bachelor's degree in a relevant scientific field

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.