Clinical Research Coordinator in Palermo
Tutte le competenze, le qualifiche e l'esperienza necessarie per un candidato di successo sono elencate nella seguente descrizione.
Working Hours: Tempo parziale, 24h 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 Palermo. This part-time 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) 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
Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
Patient education
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 xlwpduy of medical terminology
Strong 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 site
Excellent interpersonal and communication skills
Strong organizational skills and attention to detail
Fluency in Italian and good command of English
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