Clinical Research Associate

ICON plc

Clinical Research Associate monitoring ophthalmology or multi-TA trials for ICON, a global clinical research organisation. Conducting site visits, ensuring protocol compliance, and maintaining clinical data integrity.

Posted 8/14/2026full-timeRemote • Arizona, California, Colorado, Oregon • 🇺🇸 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 and monitoring, ensuring compliance with ICH-GCP guidelines and maintaining data integrity. Strong ability to collaborate with site staff and investigators while managing deliverables in a fast-paced environment.

Highest-signal resume keywords

Clinical Trial DesignICH-GCP GuidelinesOphthalmology Trials MonitoringData Integrity ManagementClinical Research Associate Experience

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial ProcessesData ReviewProtocol ComplianceStudy Documentation PreparationSite QualificationMonitoring ActivitiesClose-Out VisitsInitiation Visits

Soft Skills

Strong Organizational SkillsCommunication SkillsAttention to DetailAbility to Work IndependentlyCollaborative Skills

Industry Keywords

Clinical ResearchHealthcareScientific FieldPatient SafetyMulti-TA Trials

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 throughout trials
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 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