Clinical Research Associate

ICON plc

Clinical Research Associate contributing to clinical trial monitoring and data management for ICON. Ensuring protocol compliance and high-quality data while collaborating with investigators and site staff.

Posted 7/9/2026full-timeRemote • 🇧🇬 BulgariaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial processes, including site qualification, monitoring, and compliance with ICH-GCP guidelines. Strong organizational and communication skills are essential for maintaining data integrity and facilitating collaboration with investigators and site staff.

Highest-signal resume keywords

Clinical Trial MonitoringICH-GCP GuidelinesData IntegritySite QualificationClinical Research Associate Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesProtocol ComplianceData ReviewStudy Documentation PreparationQuery Resolution

Soft Skills

Organizational SkillsCommunication SkillsAttention to DetailCollaborative WorkIndependent Work

Industry Keywords

Clinical TrialsHealthcareScientific FieldPatient SafetyStudy Conduct

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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