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CRA at ICON plc - ApplyBlast

CRA

ICON plc

5 months ago

Remote

Full Time

Junior

0 applicants

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About this role

A UK-based Clinical Research Associate at ICON contributes to clinical trial operations by coordinating study setup, monitoring, and documentation to ensure high-quality outcomes. The role requires managing sponsor queries, preparing feasibility studies, and maintaining strong relationships with clinical investigators and site staff while ensuring patient safety and regulatory compliance. Residents of the UK with relevant monitoring experience are the primary target for this home-based position.

Responsibilities

Coordinate activities for setting up and monitoring clinical studies
Complete accurate study status reports and maintain documentation
Run sponsor-generated queries and manage study costs efficiently
Prepare and review feasibility studies for new proposals
Ensure patient safety through compliance with protocols

Skills

Qualifications

University degree in medicineUniversity degree in science

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.