Clinical Research Associate

Clinical Careers Page(2 months ago)

HybridFull TimeSenior$155,318 - $208,197 (estimated)Clinical Research

About this role

A Senior Clinical Research Associate (CRA) at ICON plc oversees and manages clinical trial activities to ensure adherence to protocol, regulatory requirements, and industry standards. The role focuses on ensuring participant safety and data integrity across study sites. It supports clinical development through collaboration with cross-functional teams and engagement with site personnel.

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Required Skills

Clinical Monitoring
Site Monitoring
Data Integrity
Regulatory Compliance
GCP
Site Management
Stakeholder Management
Communication
Project Management
Clinical Software

+2 more

Qualifications

Advanced Degree (Life Sciences/Nursing/Medicine)
Driver's License

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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