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.

📌 Clinical Research Coordinator (Milano)
🏢 Iqvia
📍 Milano