Clinical Research Associate

ICON plc

Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Ensuring protocol compliance, data integrity, patient safety, and high-quality study data.

Posted 8/22/2026full-timeRemote • Pennsylvania • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial processes, including site qualification, monitoring, and compliance with ICH-GCP guidelines. Strong organizational and communication skills are essential for effective collaboration and maintaining data integrity.

Highest-signal resume keywords

Clinical Trial MonitoringICH-GCP GuidelinesData IntegrityClinical Research Associate ExperienceProtocol Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesData ReviewStudy Documentation PreparationQuery ResolutionSite QualificationInitiation VisitsMonitoring VisitsClose-Out Visits

Soft Skills

Organizational SkillsCommunication SkillsAttention to DetailCollaborationIndependence

Industry Keywords

Clinical TrialsPatient SafetyRegulationsScientific FieldHealthcare-Related Field

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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
Contribute to clinical trial monitoring activities and take responsibility for deliverables

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%)
Legal right to work in the country where the role is based

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