CLINICAL RESEARCH ASSOCIATE
Location: Milan, Italy.
Responsibilities

Site initiation, monitoring, and close-out in accordance to GCP.
Monitoring visits and site management of national and European centres.
Tracking patient recruitment and enrollment.
Evaluating integrity and quality of patient data and investigator study file.

Qualifications

A good scientific background.
An excellent level of English, both written and spoken is a mandatory requirement.
A basic level of German language would be preferable.
The ability to travel frequently.
A high level of attention to detail.
The ability to work independently.

Benefits
A contract and salary proportional to the experience of the successful candidate.
EEO Statement
We invite interested candidates to submit their applications expressly authorizing the processing of personal data in accordance with Legislative Decree 196/2003. Our recruitment adheres to the provisions of Legislative Decree 198/2006, and we welcome applications from candidates of any gender orientation or expression, sexual orientation, age, ethnicity, or religious belief.
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