Sr. Clinical Research Associate

Clinical Careers Page(4 days ago)

TexasOnsiteFull TimeSenior$111,215 - $151,098 (estimated)Clinical Research

About this role

A Senior Clinical Research Associate at ICON plc plays a key role in site monitoring and management activities for clinical trials, ensuring compliance with regulatory standards while supporting study execution. The role involves working closely with sites across phases I-IV of drug development to maintain data quality and participant safety.

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Required Skills

GCP
ICH E6
Veeva
Edc
Ctms
Risk-Based Monitoring
Site Management
Clinical Trials
Source Data Verification
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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