Clinical Research Coordinator - part time

IQVIA seeks a Clinical Research Coordinator for a 24-hour-per-week, approximately 9-month position at a clinical research site in Verona. The role involves administrative and clinical support tasks including patient screening, documentation management, and trial operations to ensure smooth clinical trial execution.

Responsibilities

• Perform prescreening and screening tasks, including chart review from site database
• Maintain and update study documentation, including protocols, CRFs, EDC systems, and eTMFs
• Support patient screening and enrollment, handling informed consent and privacy documentation
• Operate IRT/IWRS systems for subject randomization, product assignment, and inventory management
• Coordinate logistical activities for study procedures and communicate with study monitors

Requirements

• Bachelor's degree in life sciences or equivalent education and clinical/medical experience
• Minimum 2 years as Clinical Research Assistant, Research Nurse, or Clinical Research Coordinator at a trial site
• Solid understanding of clinical trials, protocols, consent forms, and study schedules
• Experience with lab samples and IRT/IWRS systems
• Strong proficiency in MS Office applications (Outlook, Word, Excel, Access)
• Good knowledge of medical terminology and fluency in English
• Excellent interpersonal, communication, and organizational skills with strong attention to detail

Compensation: €29,800–€44,800 base (annualized)