Rome, Italy | Tempo parziale | Field-based | R1568090 Clinical Research Coordinator in Rome Working Hours: 2 hours per week Start Date: Immediately Duration: Approximately 6 months Key Responsibilities Prescreening and Screening tasks Review charts from the site data base Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems Supporting patient screening and enrollment, including handling informed consent and privacy documentation Coordinating logistical activities for study procedures in line with the study protocol Communicating with study monitors and responding to study-related inquiries Carrying out general administrative tasks related to the study Your Profile Bachelor's degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant) Solid understanding of clinical trials and familiarity with study protocols, consent forms,



and schedules Good knowledge of medical terminology Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access) Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site Excellent interpersonal and communication skills Strong organizational skills and attention to detail Fluency in English Why Join IQVIA? At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference. Where you'll work Field-based You'll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact. IQVIA is a leading glo

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