Clinical Research Associate – Sponsor Dedicated

ICON plc

Clinical Research Associate at ICON contributing to clinical trial design and analysis. Collaborating on site monitoring and ensuring data integrity while being fluent in Dutch and English.

Posted 6/10/2026full-timeRemote • 🇳🇱 NetherlandsJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout the trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolution of queries to maintain high-quality clinical data
Contribute 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%)
Fluently in Dutch and English

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