Clinical Research Associate II

ICON plc

CRA II at ICON designing and analyzing clinical trials to advance healthcare. Collaborating with clinical staff and ensuring protocol compliance during trial processes.

Posted 7/9/2026full-timeRemote • 🇵🇱 PolandJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial monitoring, ensuring protocol compliance, data integrity, and patient safety. Proficient in collaborating with site staff and investigators while maintaining high-quality clinical data throughout the trial process.

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

Site QualificationSite InitiationMonitoring VisitsClose-Out VisitsData ReviewQuery ResolutionStudy Documentation PreparationClinical Study Reports

Soft Skills

Strong Organizational SkillsCommunication SkillsAttention to DetailAbility to Work IndependentlyCollaborative Skills

Industry Keywords

Clinical Trial ProcessesHealthcare-Related FieldScientific FieldFast-Paced EnvironmentWillingness to Travel

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of 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.
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%)

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