Clinical Trial Assistant (CTA/SMA)

Clinical Careers Page(1 month ago)

HybridFull TimeJunior$60,742 - $81,471 (estimated)Clinical Operations

About this role

A Site Management Associate I at ICON supports the management of clinical trial sites by assisting with site monitoring, ensuring protocol compliance, and providing administrative and logistical support. The role contributes to clinical research success through accurate recordkeeping, data tracking, and coordination with cross-functional teams.

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Required Skills

Site Monitoring
Data Entry
Documentation
Regulatory Compliance
GCP Knowledge
Communication
Record Keeping
Organization

Qualifications

Bachelor's Degree in Life Sciences, Healthcare Administration or Clinical Research

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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