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Clinical Research Associate at ICON plc - ApplyBlast

Clinical Research Associate

ICON plc

4 months ago

Canada

Hybrid

Full Time

Junior

0 applicants

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About this role

A Clinical Research Associate at ICON conducts site visits, ensures protocol compliance, and reviews clinical trial data to support the development of new medical treatments. This role involves collaborating with investigators, resolving data queries, and preparing study documentation while adhering to regulatory guidelines. The position requires significant travel, including international flights and driving, to monitor clinical trials across various locations.

Responsibilities

Conduct site qualification, initiation, monitoring, and close-out visits
Ensure protocol compliance and data integrity throughout the trial
Collaborate with investigators and site staff on study conduct
Perform data review and resolution of clinical queries
Prepare and review study documentation and reports

Skills

Qualifications

Bachelor's degree in a scientific or healthcare-related field

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.