Clinical Research Coordinator
Pubblicato il 24-10-2026 - Iqvia in Milano
Clinical Research Coordinator – tempo parziale
Working Hours
20 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 Milano. This 20h 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:
• Prescreening and Screening tasks
• Review charts from the site data base
• Maintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and eTMFs
• Supporting patient screening and enrollment, including handling informed consent and privacy documentation
• IP
- site accountability including IP
- patient compliance
• Use of IRT/IWRS systems for subject randomization, investigational product assignment, inventory management, and site-level clinical trial operations
• Processing and shipment of lab samples process
• Patient scheduling support
• Printing and certifying EMR
• 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:
• 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
• Experience with lap samples and IRT/IWRS systems
• 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. Interested? If this sounds like the right opportunity for you, we encourage you to apply today.