Clinical Trial Assistant
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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-18808-Ljbffr
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