Clinical Site Manager II (Sr CRA)

Clinical Careers Page(2 days ago)

HybridFull TimeSenior$70,000 - $90,000Clinical Research

About this role

ICON plc is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities, ensuring regulatory compliance, data integrity, and participant safety. The role involves monitoring sites, supporting trial execution, and collaborating with cross-functional teams to achieve clinical development goals.

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Required Skills

GCP
Clinical Trials
Site Management
Monitoring
Data Integrity
Regulatory Compliance
Trial Software
Stakeholder Management
Communication
Problem Solving

Qualifications

Advanced degree in life sciences, nursing or medicine

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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