09 ago - Milano
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BeOne is seeking an experienced Clinical Research Associate to execute site monitoring and ensure trial quality across oncology studies. You will perform site selection, initiation visits, and ongoing monitoring in accordance with ICH-GCP, SOPs, and local regulations.
Strong communication with country/regional teams is essential. Qualifications include a BS in a scientific field and 3–5 years of CRA monitoring experience in pharma or CRO, with oncology trials preferred.
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