26 set - Milano
Icon Clinical
Overview
In this role you support sponsor-led clinical trials within a collaborative ICON ecosystem, contributing to design, execution, and data interpretation.
You will work with cross-functional teams to ensure compliant trial conduct, documentation, and timely milestones, helping advance innovative therapies for patients.
You will engage in regulatory submissions, study materials, and trial metrics, delivering high-quality research support in a fast-paced environment.
This position offers development in a global, patient-focused organization.
Retribuzione / Benefits
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
Responsabilità
Coordinate and administer clinical trials ensuring adherence to protocols and regulations
Organize and maintain trial documentation, essential documents, and regulatory submissions
Assist in preparing study materials such as informed consent forms and case report forms
Collaborate with cross-functional teams to enable smooth trial execution
Support tracking and reporting of trial metrics and milestones
Requisiti fondamentali
Bachelor's degree in a scientific or healthcare-related field
Prior experience or strong interest in clinical research
Knowledge of clinical trial processes, regulations, and guidelines
Excellent organizational and communication skills
Ability to work collaboratively in a fast-paced environment with attention to detail
Willingness to travel approximately 10%
organizational skills
communication skills
team collaboration
knowledge of clinical trial processes and regulations
study documentation management
regulatory submissions
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