Monitor progress of clinical studies at investigative sites.
Ensure studies are conducted, recorded and reported per protocol and ICH-GCP.
Coordinate setup and monitoring activities (investigators, submissions, visits).
Travel for site visits; remote monitoring as needed.
Support study teams to deliver quality outcomes.

🎯 Requirements

Life science degree or equivalent experience.
At least 6 months CRA experience in CRO or pharma.
Experience managing oncology studies.
Domestic travel up to 50-60% (international travel may be required).
Fluency in English and Italian.

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