IQVIA seeks a Clinical Research Coordinator for a clinical trial site in Pisa, working 9 hours per week for approximately ***** months. The role involves administrative and clinical support, including patient screening, documentation management, and coordination of study procedures.
Responsibilities
Perform prescreening and screening tasks, including chart review and patient screening support
Maintain and update study documentation, protocols, case report forms, EDC systems, and eTMFs
Handle informed consent, privacy documentation, and investigational product accountability
Manage 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 experience
2–3 years experience as Clinical Research Assistant, Research Nurse, or Clinical Research Coordinator
Understanding of clinical trials, protocols, consent forms, and study schedules
Experience with lab samples and IRT/IWRS systems
Proficiency in MS Office applications and strong IT skills
Knowledge of medical terminology and fluency in English
Excellent interpersonal, communication, and organizational skills
Compensation:
€29,800–€44,800 base (annualized)

📌 Clinical Research Coordinator In Pisa - Part Time
🏢 Iqvia
📍 Pisa