Part-Time Clinical Research Coordinator (6-Month)

IQVIA; Milano; On-site; EUR 30,000 - 45,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator in Milano to support a clinical trial site. The role offers 10 hours per week for approximately six months, starting immediately.

Responsibilities include prescreening, chart reviews, documentation, patient screening and consent, IP accountability, and site operations. The candidate should have a life sciences degree or equivalent, at least 2 years of site experience, English fluency, and strong IT skills (MS Office).

Qualifications

• Bachelor’s degree in life sciences or equivalent education/experience.
• Minimum 2 years of experience as a Clinical Research Assistant, Research Nurse or CRC at a clinical trial site.
• Fluent in English with strong communication skills.
• Strong IT skills including MS Office (Outlook, Word, Excel, Access).

Responsibilities

• Pre-screening and screening tasks.
• Review charts from the site database.
• Maintain and update study documentation (protocols, CRFs, EDC, eTMFs).
• Support patient screening and enrollment, including informed consent and privacy documentation.
• IP-site accountability including IP-patient compliance.
• Use of IRT/IWRS for subject randomization, product assignment, inventory, and site operations.
• Process and shipment of lab samples.
• Coordinate patient scheduling and EMR printing/certification.
• Coordinate study logistics per protocol and communicate with monitors.
• Carry out general administrative tasks for the study.

Skills

Clinical research

English fluency

MS Office

Education

Bachelor’s degree in life sciences

Tools

IRT/IWRS

EMR

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator in Milano to support a clinical trial site. The role offers 10 hours per week for approximately six months, starting immediately.

Responsibilities include prescreening, chart reviews, documentation, patient screening and consent, IP accountability, and site operations. The candidate should have a life sciences degree or equivalent, at least 2 years of site experience, English fluency, and strong IT skills (MS Office).