Sr. Clinical Research Associate

Clinical Careers Page(4 days ago)

North CarolinaOnsiteFull TimeSenior$101,402 - $138,441 (estimated)

About this role

A Senior Clinical Research Associate at ICON plc specializes in site monitoring and management activities for clinical trials across various phases. They ensure compliance with industry standards, support study execution, and maintain high-quality data and participant safety while collaborating with site personnel and study teams.

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Required Skills

Veeva EDC
CTMS
Risk-Based Monitoring
Site Management
Data Verification
Source Data Review
Regulatory Compliance
Study Conduct
Clinical Trials
Monitoring

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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