12 set - Roma
Iqvia
Clinical Research Coordinator in Rome Working Hours: 2 hours per week Start Date: Immediately Duration: Approximately 6 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Rome. This only 2 hour per week role offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.
Qualifiche, competenze e l'esperienza necessaria per questo ruolo sono disponibili nella descrizione completa riportata di seguito.
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 project
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