Part-Time Clinical Research Coordinator – Verona

IQVIA Inc; Veneto; Hybrid; EUR 30,000 - 45,000; Part time

Job summary

IQVIA is recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Verona. This part-time role (24 hours per week) starts immediately and runs for approximately nine months.

You will contribute to meaningful research in a collaborative, dynamic environment. Responsibilities include prescreening, reviewing site charts, maintaining study documentation, assisting with patient screening and consent, and coordinating procedures with monitors.

Qualifications

• Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting.
• Experience with clinical trials, study protocols, and schedules.
• Fluency in English and excellent interpersonal communication.
• Experience with IRT/IWRS systems and EDC systems.
• Strong organizational skills and attention to detail.

Responsibilities

• Prescreening and Screening tasks
• Review charts from the site data base
• Maintaining and updating study documentation, including protocols, CRFs, EDCs and eTMFs
• Supporting patient screening and enrollment, including informed consent and privacy documentation
• Use of IRT/IWRS systems for subject randomization, product assignment, inventory management, and site-level trial operations
• Patient scheduling support
• Coordinating logistical activities for study procedures per protocol
• Communicating with study monitors and responding to inquiries
• Carrying out general administrative tasks related to the study

Skills

English fluency

Interpersonal communication

Organizational skills

Attention to detail

Medical terminology knowledge

Education

Bachelor’s degree in life sciences

Tools

MS Office (Outlook, Word, Excel, Access)

IRT/IWRS systems

EDC systems

Job description

IQVIA is recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Verona. This part-time role (24 hours per week) starts immediately and runs for approximately nine months.

You will contribute to meaningful research in a collaborative, dynamic environment. Responsibilities include prescreening, reviewing site charts, maintaining study documentation, assisting with patient screening and consent, and coordinating procedures with monitors.