Clinical Trial Assistant

05 ott - Turbigo
Planet Pharma

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

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Key Responsibilities:

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- 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:

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- 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.

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