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Clinical Study Specialist (Hybrid) at ICON plc - ApplyBlast

Clinical Study Specialist (Hybrid)

ICON plc

2 months ago

Cambridge, Massachusetts, United States

Hybrid

Full Time

Junior

0 applicants

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About this role

The Clinical Study Specialist supports global clinical trials by organizing reports, coordinating meetings, managing study documentation, and tracking site activities. The role involves maintaining trial master file compliance, facilitating vendor oversight, and contributing to process improvements within a hybrid work environment.

Responsibilities

Organize and deliver analyzable reports and metrics to clinical study lead
Track site activation, enrollment and monitoring visits and escalate issues
Manage and maintain study Trial Master File reconciliations

Skills

Qualifications

Bachelor's Degree

About ICON plc

iconplc.com

Headquarters

South Dublin, Ireland

Company Size

10001+ employees

Founded

1990

View Profile

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.