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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