Clinical Research Associate

ICON plc

Clinical Research Associate at ICON responsible for designing and analyzing clinical trials. Ensuring protocol compliance, data integrity, and patient safety while collaborating with investigators.

Posted 6/26/2026full-timeRemote • 🇫🇷 FranceJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Contributing to clinical trial monitoring activities, taking responsibility for deliverables and working collaboratively
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
Collaborating with investigators and site staff to facilitate smooth study conduct
Performing data review and resolution of queries to maintain high-quality clinical data
Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Requirements

What you’ll need

Bachelor's degree in a scientific or healthcare-related field
Minimum of 2 years of experience as a Clinical Research Associate
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills, with attention to detail
Ability to work independently and collaboratively in a fast-paced environment
Willingness to travel as required (approximately 60%)

Benefits

Comp & perks

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trial monitoringsite qualificationdata reviewprotocol compliancedata integritypatient safetystudy documentation preparationclinical study reportsquery resolutionICH-GCP guidelines

Soft Skills

organizational skillscommunication skillsattention to detailindependent workcollaborative workadaptabilityproblem-solvingtime managementinterpersonal skillsteamwork