Clinical Study Specialist (hybrid/Office-based - Warren, NJ or Cambridge MA)

Clinical Careers Page(1 month ago)

HybridFull TimeMedior$89,167 - $119,240 (estimated)Clinical Operations

About this role

A Clinical Study Specialist at ICON plc supports the execution and oversight of global clinical trials, ensuring study documentation and communications are maintained to support regulatory and operational needs. The role interfaces with study teams and external sites to help maintain trial integrity and facilitate study deliverables.

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Required Skills

TMF
CTMS
SharePoint
ICF Review
PowerPoint
Excel
Meeting Minutes
Vendor Management
Site Management
Enrollment Tracking

+2 more

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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