Clinical Site Associate
Clinical Careers Page(1 month ago)
About this role
A Clinical Site Associate at ICON supports clinical trial operations from the Milan office, contributing to the delivery of high-quality clinical research. The role focuses on maintaining site and trial documentation and collaborating with clinical teams to ensure trials progress smoothly. This is an office-based role with a hybrid working arrangement.
Required Skills
- Site Management
- Document Management
- TMF Management
- Site Training
- Systems Access
- Audit Readiness
- Communication
- Organization
- Attention To Detail
- Clinical Research
+2 more
Qualifications
- Bachelor's Degree in Life Sciences or Healthcare
About Clinical Careers Page
iconplc.comICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.
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