Clinical Trial Assistant (sponsor dedicated)

Clinical Careers Page(28 days ago)

Prague, Czech Republic, Czech RepublicOnsiteFull TimeJunior$35,891 - $49,295 (estimated)Clinical Research

About this role

A Clinical Trial Administrator at ICON supports the clinical development lifecycle within a global healthcare intelligence and clinical research organization. The role focuses on maintaining study documentation, supporting regulatory submissions, and facilitating communication across study teams to ensure high-quality trial execution.

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Required Skills

Clinical Trials
Regulatory Compliance
Document Management
Informed Consent
Collaboration
Reporting
Communication
Organization
Data Interpretation

Qualifications

Bachelor's Degree

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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