Are you a talented Clinical Trial Assistant with a passion for clinical research? We're looking for an experienced Freelance CTA to join a dynamic team supporting cutting-edge studies Key Responsibilities: Assist in the management and oversight of clinical trials across various therapeutic areas, including ophthalmology , neurology , and rare diseases . Support Clinical Research Associates (CRAs) and Regulatory and Start-Up Specialists (RSU) with study documentation, site compliance, and study performance tracking. Prepare, distribute, and archive clinical trial documentation in line with standard operating procedures. Assist in the preparation and maintenance of clinical trial supplies, site communications, and regulatory submissions. Review study files for completeness and accuracy , ensuring compliance with study protocols and good clinical practice (GCP). What We’re Looking For: 5+ years of experience as a Clinical Trial Assistant (CTA) or similar role within CRO or pharmaceutical environments. Hands-on experience supporting global clinical project teams and understanding of clinical trial operations. Strong knowledge of clinical trial systems like eTMF and Veeva Vault (or similar). A background in ophthalmology , neurology , or rare disease studies is preferred but not essential. Ability to work full-time on a 12-month contract . Must be able to work onsite in Milan at least 3 days per week . Fluency in English (B2 level or higher), with strong written and verbal communication skills. #J-18808-Ljbffr