Clinical Research Associate

ICON plc

Clinical Research Associate monitoring ophthalmology and multi-TA trials for ICON, a global healthcare intelligence and clinical research organization. Supporting compliant study conduct and high-quality clinical data.

Posted 8/14/2026full-timeRemote • California, Idaho, Nevada, Washington • 🇺🇸 United StatesJuniorMid-Level💰 $91,336 - $114,170 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial processes, including site qualification, monitoring, and compliance with ICH-GCP guidelines. Strong ability to collaborate with investigators and site staff while ensuring data integrity and patient safety.

Highest-signal resume keywords

Clinical Trial MonitoringICH-GCP GuidelinesOphthalmology Trials ExperienceData Integrity ManagementBachelor's Degree in Scientific Field

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesProtocol ComplianceData ReviewStudy Documentation PreparationClinical Study Reports

Soft Skills

Strong Organizational SkillsCommunication SkillsAttention to DetailAbility to Work IndependentlyCollaborative Work Style

Industry Keywords

Clinical Research AssociatePatient SafetySite QualificationMonitoring VisitsFast-Paced Environment

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
Take responsibility for clinical trial monitoring deliverables and work collaboratively
Travel as required, approximately 60%

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
Experience monitoring Ophthalmology trials or multi-TA
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
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
Reasonable accommodations during the recruitment process
Inclusive and accessible workplace