Clinical Research Associate

ICON plc

Clinical Research Associate monitoring ophthalmology and multi-TA clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Ensuring compliant study conduct, data integrity, patient safety, and high-quality clinical data.

Posted 8/14/2026full-timeRemote • Florida, Illinois, Missouri, Texas • 🇺🇸 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 design, monitoring, and compliance with ICH-GCP guidelines, ensuring data integrity and patient safety. Strong ability to collaborate with site staff and investigators while maintaining high-quality clinical data.

Highest-signal resume keywords

Clinical Trial DesignICH-GCP GuidelinesOphthalmology Trials MonitoringData IntegrityClinical Research Associate Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesData ReviewProtocol ComplianceSite QualificationMonitoring Activities

Soft Skills

Strong Organizational SkillsCommunication SkillsAttention to DetailAbility to Work IndependentlyCollaborative Skills

Industry Keywords

Clinical ResearchPatient SafetyStudy DocumentationClinical Study ReportsMulti-TA Experience

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Design and analyze clinical trials, interpreting complex medical data
Contribute to clinical trial monitoring activities and take responsibility for deliverables
Conduct site qualification, initiation, monitoring, and close-out visits
Ensure protocol compliance, data integrity, and patient safety
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolve queries to maintain high-quality clinical data
Contribute to preparing and reviewing 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
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
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