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

Scopra se questa possibilità è adatta a lei leggendo tutte le informazioni riportate di seguito.
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. xysqume

- Fluency in English (B2 level or higher), with strong written and verbal communication skills.

#J-18808-Ljbffr

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