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-*****-Ljbffr

📌 Clinical Trial Assistant (Bardi)
🏢 Planet Pharma
📍 Bardi