Clinical Research Associate

Clinical Careers Page(6 days ago)

HybridFull TimeMedior$80,890 - $108,863 (estimated)Research

About this role

A Clinical Research Associate at ICON plc oversees and coordinates clinical trials to ensure compliance with regulations and collects critical data. The role involves working independently on study setup, monitoring, and maintaining documentation, supporting clinical investigations and stakeholder relationships, and ensuring patient safety.

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Required Skills

clinical Trials
Regulatory Compliance
Data Analysis
Study Coordination
ICH-GCP
Medical Data Review
Communication Skills
Travel Management
Stakeholder Engagement
Clinical Monitoring

Qualifications

University degree in medicine, science, or equivalent

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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