Clinical Research Coordinator in PalermoWorking Hours: Part-time, 24h per weekStart Date: ImmediatelyDuration: Approximately 6 monthsIQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Palermo. This tempo parziale position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.Key Responsibilities
Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systemsSupporting patient screening and enrollment, including handling informed consent and privacy documentationCoordinating logistical activities for study procedures in line with the study protocolPerforming data entry, quality checks, and resolving queries to ensure data accuracy and completenessPatient educationCommunicating with study monitors and responding to study-related inquiriesCarrying 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 schedulesGood knowledge of medical terminologyStrong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial siteExcellent interpersonal and communication skillsStrong organizational skills and attention to detailFluency in Italian and good command of English
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