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 Pisa.
This role is for
* 20-40
* hours
* per week and is expected to last approximately 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
* 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 with good English language skills
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