FSA-Site Specialist Ⅰ, Site Specialist II and Senior Site Specialist

ICON plc

8 months ago

Tokyo, Japan

Hybrid

Full Time

Medior

0 applicants

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About this role

A Site Specialist at ICON supports the clinical development process by managing regulatory and site-level documentation required for study initiation. The role ensures compliance with sponsor and ICON SOPs, applicable regulations and ICH/GCP, while contributing to quality improvement and process enhancements to meet client expectations.

Skills

Qualifications

Bachelor’s Degree

About ICON plc

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.