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

📌 Clinical Trial Associate (Italia)
🏢 Icon Clinical
📍 Italia