Sr. Clinical Research Associate

Icon Clinical PLC

Industria de Investigación Farmacéutica

20095 Milanino, Lombardia - Italien

Project Manager Sénior / Especialista sénior

Experteer Overview

As a Senior CRA at ICON, you oversee clinical trial activities to ensure protocol adherence, regulatory compliance, and data integrity. You will support site visits, train staff, and collaborate with cross-functional teams to drive smooth trial execution. The role is pivotal in safeguarding participant safety and trial quality across sites and studies. You will work within a diverse, inclusive culture that values excellence and impactful clinical development.

Compensaciones / Beneficios

annual leave entitlements
health insurance offerings
retirement planning options
Global Employee Assistance Programme LifeWorks
life assurance
flexible country-specific optional benefits

Responsabilidades

Monitor trial sites for protocol, regulatory, and GCP compliance
Conduct site visits to assess performance and resolve issues
Collaborate with cross-functional teams to ensure timely data collection and reporting
Provide training and guidance to site staff and other CRAs
Build and maintain relationships with site personnel and stakeholders to enable smooth operations

Requisitos principales

Advanced degree in a relevant field (life sciences, nursing, or medicine)
Extensive experience as a Clinical Research Associate with strong regulatory knowledge
Ability to manage multiple sites and projects with organizational and problem-solving skills
Expertise in monitoring, data integrity, and site management; proficiency with clinical trial software/tools
Excellent communication, interpersonal, and stakeholder management skills; capable of driving compliance in a complex environment
Ability to travel at least 60% with a valid driver's license

strong communication stakeholder management problem-solving monitoring practices data integrity site management

Descripción del puesto

As a Senior CRA at ICON, you oversee clinical trial activities to ensure protocol adherence, regulatory compliance, and data integrity. You …

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