Clinical Study Specialist

ICON plc

12 days ago

Basking Ridge, NJ

Hybrid

Full Time

Medior

0 applicants

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About this role

ICON plc is seeking a Clinical Study Specialist responsible for organizing and delivering reports, coordinating meetings, and supporting various study activities for clinical trials. The role involves managing study documentation, site and trial monitoring, and ensuring compliance with standard operating procedures.

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.