Clinical Research Associate

Clinical Careers Page(1 day ago)

Chicago, ILOnsiteFull TimeMedior$60,000 - $75,000Clinical Research

About this role

A Clinical Research Associate at ICON focuses on the start-up phase of oncology clinical trials, working closely with site staff and cross-functional teams to activate trial sites and ensure compliance with regulatory standards. The role involves site qualification, documentation, and collaboration to support successful trial initiation.

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Required Skills

Clinical Trials
Site Management
Regulatory Compliance
GCP
Site Qualification
Oncology
Study Start Up
Documentation
Monitoring
Regulatory Standards

About Clinical Careers Page

iconplc.com

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.

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