pWe are partnering with a leading CRO to recruit both a bClinical Research Associate II /b and a bSenior Clinical Research Associate /b 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.
/ppbr/ppThis is an excellent opportunity to join a collaborative clinical operations team working on innovative Phase I–IV studies across oncology.
/ppbr/ppbKey Responsibilities /b /ppbr/pulliIndependently manage assigned investigative sites throughout the full clinical trial lifecycle.
/liliConduct bSite Selection Visits (SSVs), Pre-Study Visits (PSVs), Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs) /b and bClose-Out Visits (COVs) /b.
/liliEnsure studies are conducted in accordance with ICH-GCP, protocol requirements, SOPs and applicable regulatory guidelines.

/liliMaintain strong relationships with investigators, site staff and sponsor representatives.
/liliPerform Source Data Verification (SDV) and Source Data Review (SDR) while ensuring high data quality.
/liliIdentify, document and escalate protocol deviations and study risks where appropriate.
/liliReview and maintain Investigator Site Files (ISFs), Trial Master Files (TMFs) and essential documentation.
/liliSupport patient recruitment and retention strategies with investigative sites.
/liliEnsure sites remain inspection and audit ready throughout the duration of the study.
/liliWork collaboratively with Clinical Trial Managers, Project Managers and cross-functional teams to ensure successful study delivery.
/li /ulpbr/p

Clinical Research Associate Ii / Senior Cra

Consulente Tricologa/o

QC Analyst Junior

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