Descrizione:
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).
- 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.
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