15 ott - Roma
Iqvia
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
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