Clinical Research Associate – Oncology Trials (Global, Travel)

Worldwide Clinical Trials

Italia

On-site

EUR 40,000 - 60,000

Full time

14 days+

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Job summary

Worldwide Clinical Trials in Italy is seeking a Clinical Research Associate (CRA) to work with brilliant minds across Oncology, Neuroscience, Cardiovascular, Metabolic and Rare Diseases. You will support sites, ensure protocol adherence, and contribute to TMF management and data quality.

The role requires 2+ years as a CRA, a 4-year degree or RN/BSN, willingness to travel, and proficiency in Microsoft Office, CTMS and EDC systems.

Qualifications

2+ years of experience as a Clinical Research Associate.
Experience in Oncology and Hematology is required.
Willingness to travel required.

Responsibilities

Site qualification, initiation, interim monitoring, site management, and study close‑out visits.
Provide mentoring and guidance to less experienced CRAs and site staff when needed.
Document site visit findings via written reports.
Assess, monitor, and train study site staff on protocol adherence as required.
Review study subject safety information and informed consent.
Conduct source document verification for compliance, patient safety, and veracity of data.
Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
Provide applicable updates for site related documentation for filing in the Trial Master File (TMF).
Ensure site compliance with IP receipt, accountability and return or destruction.
Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.