Clinical Research Coordinator in Rome

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Working Hours: 2 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 Rome. This only 2 hour per week role offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.

Key Responsibilities
As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:

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- 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
We are looking for candidates who bring a combination of education, experience, and skills:

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- 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 tria

📌 Clinical Research Coordinator (Roma)
🏢 Iqvia Argentina
📍 Roma