Clinical Research Associate I

ICON plc

Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Coordinating study setup, monitoring, documentation, and stakeholder relationships.

Posted 8/21/2026full-timeRemote • 🇦🇷 ArgentinaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial monitoring, ensuring compliance with ICH-GCP guidelines and maintaining study documentation. Capable of developing collaborative relationships with stakeholders while ensuring patient safety and cost efficiency.

Highest-signal resume keywords

Clinical Trial Monitoring ExperienceICH-GCP Guidelines KnowledgeMedical Data Review ExpertiseExcellent Written And Verbal CommunicationStakeholder Relationship Development

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

Study Documentation MaintenanceStudy Status ReportingQuery ManagementCost Efficiency ManagementFeasibility Study Preparation

Soft Skills

Good Social SkillsTimely Query Resolution

Industry Keywords

Patient SafetyRegulatory ComplianceClinical InvestigatorsSite StaffUniversity Degree In Medicine Or Science

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Coordinate all activities for setting up and monitoring a study
Complete accurate study status reports and maintain study documentation
Run sponsor generated queries efficiently
Take responsibility for study cost efficiency
Participate in the preparation and review of study documentation and feasibility studies for new proposals as required
Develop and maintain collaborative relationships with key stakeholders, clinical investigators, and site staff
Ensure patient safety and compliance with ICON's procedures, protocols, and regulatory requirements

Requirements

What you’ll need

University degree in medicine, science, or equivalent
Relevant clinical trial monitoring experience
Knowledge of ICH-GCP guidelines
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 35%)
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