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Clinical Associate at ICON plc - ApplyBlast

Clinical Associate

ICON plc

3 months ago

United States

Onsite

Full Time

Junior

0 applicants

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About this role

As a Clinical Associate at ICON, you will support the execution and management of clinical trials across all phases, ensuring quality, efficiency, and compliance. The role involves coordinating site feasibility, managing trial budgets, overseeing the Trial Master File, and tracking investigational product supplies to advance innovative treatments.

Responsibilities

Support planning and execution of clinical trials across phases
Maintain and analyze trial tracking systems for data accuracy
Track and analyze trial budgets with variance reporting
Manage the Trial Master File for inspection readiness
Coordinate site feasibility assessments and regulatory documentation

Skills

Qualifications

Bachelor's degree in life sciences or healthcarePrevious experience in clinical research

About ICON plc

iconplc.com

Headquarters

South Dublin, Ireland

Company Size

10001+ employees

Founded

1990

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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.