Clinical Research Associate

ICON plc

Clinical Research Associate at ICON designing and analyzing clinical trials for healthcare advancements. Monitoring trial activities and ensuring compliance with data integrity and patient safety.

Posted 7/7/2026full-timeRemote • 🇮🇹 ItalyJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial monitoring, ensuring compliance with ICH-GCP guidelines and ICON's procedures. Strong ability to coordinate study activities, maintain documentation, and foster collaborative relationships with stakeholders.

Highest-signal resume keywords

Clinical Trial MonitoringICH-GCP GuidelinesStudy Documentation ManagementExcellent Written And Verbal CommunicationStakeholder Relationship Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial MonitoringStudy Documentation ManagementMedical Data EvaluationFeasibility Study PreparationCost Efficiency Management

Soft Skills

Excellent Written And Verbal CommunicationGood Social Skills

Industry Keywords

Patient SafetyRegulatory ComplianceUniversity Degree In MedicineUniversity Degree In ScienceTravel Willingness

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Delivering clinical trial monitoring work to a high standard
Working independently and actively to coordinate all activities for setting up and monitoring a study
Completing accurate study status reports and maintaining study documentation
Running sponsor generated queries efficiently and taking responsibility for study cost efficiency
Participating in the preparation and review of study documentation and feasibility studies for new proposals as required
Developing and maintaining strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
Ensuring patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements

Requirements

What you’ll need

University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
Excellent written and verbal communication in English
Good social skills enabling you to deal with queries in a timely manner
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