Clinical Research Coordinator - Palermo

Working Hours: Part-time, 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.

• 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

• 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 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