Clinical Research Coordinator
Pubblicato il 18-09-2026 - Iqvia in Roma
Rome, Italy | Tempo parziale | Field-based | R Clinical Research Coordinator in Rome Working Hours: 2 hours per week Start Date: Immediately Duration: Approximately 6 months
Key Responsibilities
- Prescreening and Screening tasks
- Review charts from the site data base
- 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
- 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 of medical terminology
- Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
- Must have at least 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 English
Why Join IQVIA?
At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.
Where you’ll work
Field-based You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impac