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)

📌 Clinical Research Coordinator - Part Time (Verona)
🏢 Iqvia
📍 Verona