We are partnering with a leading CRO to recruit both a Scopra di più sui compiti quotidiani, le responsabilità generali e l'esperienza richiesta per questa occasione scorrendo subito verso il basso.
Clinical Research Associate II
Senior Clinical Research Associate
to support a growing portfolio of clinical studies across Italy. These are home-based positions covering sites primarily within Northern Italy, with an emphasis on high-quality site management and sponsor collaboration.
This is an excellent opportunity to join a collaborative clinical operations team working on innovative Phase I–IV studies across oncology.
Independently manage assigned investigative sites throughout the full clinical trial lifecycle.
Site Selection Visits (SSVs),

Pre-Study Visits (PSVs), Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs)
Ensure studies are conducted in accordance with ICH-GCP, protocol requirements, SOPs and applicable regulatory guidelines.
Perform Source Data Verification (SDV) and Source Data Review (SDR) while ensuring high data quality.
Ensure sites remain inspection and audit ready throughout the duration of the study. Work collaboratively with Clinical Trial Managers, Project Managers and cross-functional teams to ensure successful study delivery.

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