Clinical Research Coordinator

18 set - Roma
Iqvia

Rome, Italy | Tempo parziale | Field-based | R1568090 Clinical Research Coordinator in Rome Working Hours: 2 hours per week Start Date: Immediately Duration: Approximately 6 months

Qualifiche, competenze e l'esperienza necessaria per questo ruolo sono disponibili nella descrizione completa riportata di seguito.
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 workField-based You’ll work where the action is — out in the field, directly engaging with our customers, sites or

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