Part-Time Clinical Research Coordinator (Pisa)

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

Job summary

IQVIA is recruiting a Clinical Research Coordinator to support a clinical research site in Pisa. The role is 9 hours per week with immediate start and a duration of approximately 10-11 months.

The candidate will prescreen, review charts, maintain study documents, and assist with patient screening and enrollment, along with IRT/IWRS usage and lab sample handling. Strong English and IT skills are required.

Qualifications

• Bachelor’s degree in life sciences or equivalent.
• Solid understanding of clinical trials and study protocols.
• Experience with IRT/IWRS systems.
• Good knowledge of medical terminology.
• Excellent interpersonal and communication skills.
• Fluency in English.

Responsibilities

• Pre-screening and screening tasks as part of site activities.
• Review charts from the site database to support data accuracy.
• Maintain and update study documentation (protocols, CRFs, EDC, eTMF).
• Assist with patient screening and enrollment, including informed consent.
• Support IP-site accountability and patient compliance.
• Utilize IRT/IWRS systems for subject randomization and product inventory.
• Process and arrange shipping of lab samples.
• Schedule patients and coordinate study procedures.
• Print and certify EMR entries and maintain documentation.
• Coordinate logistics for study procedures per protocol.
• Communicate with monitors and respond to inquiries.
• Perform general study-related administrative tasks.

Skills

Fluency in English

Interpersonal skills

Organizational skills

Attention to detail

Communication skills

Education

Bachelor's degree in life sciences

Tools

MS Office

Job description

IQVIA is recruiting a Clinical Research Coordinator to support a clinical research site in Pisa. The role is 9 hours per week with immediate start and a duration of approximately 10-11 months.

The candidate will prescreen, review charts, maintain study documents, and assist with patient screening and enrollment, along with IRT/IWRS usage and lab sample handling. Strong English and IT skills are required.