IQVIA is seeking a tempo parziale Clinical Research Coordinator to support a Rome site.
The role involves prescreening, reviewing charts, maintaining study documentation, and assisting with patient enrollment, consent, and privacy paperwork.
Requirements include a life sciences degree, at least 2 years of clinical trial site experience, strong IT skills, and fluency in English.
This 2-hour-per-week position offers exposure to global clinical research operations and data capture systems.
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