At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.
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As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that agevolazioni patients worldwide.
What You Will Do
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key Responsibilities Include
- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.




- Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile
You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required Qualifications And Experience
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
- Excellent communication, interpersonal,

📌 Senior Clinical Research Associate (Milano)
🏢 ICON San Antonio
📍 Milano