Clinical Research Associate

ICON plc

. Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials .

Posted 9/30/2026full-timeRemote • SpainJuniorMid-LevelWebsite

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 analyze complex medical data and contribute to high-quality clinical documentation and innovative treatments.

Highest-signal resume keywords

Clinical Trial ProcessesICH-GCP GuidelinesData IntegrityClinical Research Associate ExperienceStudy Documentation Preparation

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 DesignData ReviewProtocol CompliancePatient SafetyMedical Data Analysis

Soft Skills

Organizational SkillsCommunication SkillsAttention to DetailCollaborative WorkIndependent Work

Industry Keywords

Clinical TrialsSite QualificationMonitoring VisitsStudy ReportsRegulatory Compliance

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
Design and analyse clinical trials, interpret complex medical data, and contribute to innovative treatments and therapies

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