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Site Specialist I at ICON plc - ApplyBlast

Site Specialist I

ICON plc

4 months ago

Hybrid

Full Time

Junior

0 applicants

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About this role

As a Site Specialist I at ICON, you will support investigator sites with key administrative and operational activities to ensure clinical trials run smoothly and in compliance. The role involves managing site documentation, maintaining trial management systems, and collaborating with project teams and Clinical Research Associates to resolve site queries. This position requires a supportive approach to help investigators navigate trial processes while adhering to Good Clinical Practice (GCP) principles and SOPs.

Responsibilities

Support collection, review, and tracking of essential site documents
Maintain accurate site information in clinical trial management systems
Assist with scheduling site meetings and follow-up actions
Prepare materials for site visits and audit inspections
Collaborate with CRAs to resolve basic site queries

Skills

Qualifications

BS in Life SciencesBS in HealthcareBS in BusinessGCP Knowledge

About ICON plc

iconplc.com

Headquarters

South Dublin, Ireland

Company Size

10001+ employees

Founded

1990

View Profile

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.