Part-Time Clinical Research Coordinator - Pisa

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

Job summary

IQVIA is recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Pisa. This role offers 9h per week and involves prescreening, data review, and study documentation across EDC/eTMF systems, ensuring protocol compliance and patient privacy.

We seek candidates with 2–3 years at a clinical trial site, strong IT skills, and excellent communication in English. Expect collaboration with monitors and site staff in an onsite role.

Qualifications

• Bachelor's degree in life sciences or equivalent education and/or relevant experience.
• Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules.
• Experience with lab samples and IRT/IWRS systems.
• Good knowledge of medical terminology.
• Strong IT skills, including proficiency in MS Office applications.
• Must have at least 2-3 years experience as a CRC/CRA at a trial site.
• Excellent interpersonal and communication skills.
• Fluency in English.

Responsibilities

• Prescreening and screening tasks.
• Review charts from the site data base.
• Maintaining and updating study documentation, including protocols, CRFs, EDC, 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, inventory management, and site-level trial operations.
• Processing and shipment of lab samples.
• Patient scheduling support.
• Printing and certifying EMR.
• 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

MS Office

Strong communication

Attention to detail

Interpersonal skills

Education

Bachelor’s degree in life sciences

Tools

IRT/IWRS systems

EDC systems

eTMF

Job description

IQVIA is recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Pisa. This role offers 9h per week and involves prescreening, data review, and study documentation across EDC/eTMF systems, ensuring protocol compliance and patient privacy.

We seek candidates with 2–3 years at a clinical trial site, strong IT skills, and excellent communication in English. Expect collaboration with monitors and site staff in an onsite role.