Central Review Coordinator

ICON plc

Central Review Coordinator facilitating the coordination and execution of clinical trial review activities at ICON. Ensuring data accuracy and compliance while collaborating with diverse stakeholders.

Posted 7/11/2026full-timeRemote • 🇷🇴 RomaniaMid-LevelSeniorWebsite

About the role

Key responsibilities & impact

Facilitate the coordination and execution of centralized review activities for clinical trials
Coordinate the scheduling, logistics, and execution of central review activities
Collaborate closely with study teams, clinical sites, and external vendors
Monitor the progress and quality of central review processes
Maintain comprehensive documentation and records of central review activities
Provide support and guidance to internal and external stakeholders

Requirements

What you’ll need

Bachelor's degree in life sciences, computer science, or a related discipline
Previous experience in clinical research, data management, or study coordination within the pharmaceutical, biotechnology, or CRO industry
Strong organizational and project management skills
Excellent attention to detail and problem-solving abilities
Effective communication and interpersonal skills

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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Clinical Trial CoordinationCentral Review ActivitiesDocumentation ManagementLogistics CoordinationQuality Monitoring

Soft Skills

Organizational SkillsProblem-Solving AbilitiesInterpersonal Skills