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CRA II and SR CRA at ICON plc - ApplyBlast

CRA II and SR CRA

ICON plc

3 months ago

Remote

Full Time

Senior

0 applicants

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About this role

A Clinical Research Associate II or Senior CRA at ICON delivers high-quality clinical trial monitoring work, coordinating study setup and visits while ensuring patient safety and regulatory compliance. The role involves developing strong relationships with clinical investigators and site staff, managing study documentation, and optimizing study costs. Candidates must have prior onsite monitoring experience and the ability to travel approximately 60% of the time.

Responsibilities

Coordinate all activities for setting up and monitoring clinical studies
Ensure patient safety through compliance with protocols and regulatory requirements
Develop and maintain relationships with clinical investigators and site staff
Run sponsor-generated queries efficiently and manage study cost efficiency
Prepare and review study documentation and feasibility studies for new proposals

Skills

Qualifications

University degree in medicine or science

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.