Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Venice Mestre. This role with an immediate start is for 24hoursper week and is expected to last around one year. As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including: - Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents - Support with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.); - Planning and coordinating logístical activity for study procedures according to the study protocol - Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness - Management and shipment of biological samples - Performing ECG, taking vital signs, phlebotomy - Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions - Administrative research task - BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession - Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules - Basic knowledge of medical terminology - Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients - Good organizational skills with the ability to pay close attention to detail - Fluent Italian language skills LI-CES LI-NS1 LI-HCPN LI-DNP