Clinical Trial Assistant

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.