Descrizione:
Clinical Research Coordinator – Firenze
Working Hours: Part-time, 10 hours per week
Start Date: Immediately
Duration: Approximately 6 months
IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Firenze. This part‑time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.
Key Responsibilities
Maintain and update study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems.
Support patient screening and enrollment, including handling informed consent and privacy documentation.
Coordinate logistical activities for study procedures in line with the study protocol.
Perform data entry, quality checks, and resolve queries to ensure data accuracy and completeness.
Provide patient education.
Communicate with study monitors and respond to study‑related inquiries.
Carry out general administrative tasks related to the study.
Required 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).
At least 1–2 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 Italian and good command of English.
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