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Clinical Research Associate at ICON plc - ApplyBlast

Clinical Research Associate

ICON plc

4 months ago

Quebec City, Quebec

Onsite

Full Time

Executive

0 applicants

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About this role

This role involves conducting site qualification, initiation, and monitoring visits for clinical trials while ensuring protocol compliance and data integrity. The Clinical Research Associate will collaborate with investigators to facilitate smooth study conduct and resolve clinical data queries. Based in Quebec City with up to 60% travel, the position requires a strong understanding of clinical trial processes and ICH-GCP guidelines.

Responsibilities

Conduct site qualification, initiation, and close-out visits for clinical trials
Ensure protocol compliance and data integrity throughout the trial process
Collaborate with investigators to facilitate smooth study conduct
Perform data review and resolve clinical queries to maintain data quality
Prepare and review study documentation including protocols and clinical study reports

Skills

Qualifications

Bachelor's degree in 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.