Research Nurse/Clinical Research Coordinator (Tempo parziale, On-site, Independent Contractor) Novara Italy RapidTrials is hiring an experienced Clinical Research Coordinator (CRC) to support prescreening and recruitment activities for a Phase III MASH (Metabolic Dysfunction-Associated Steatohepatitis) clinical trial. This part‐time, freelance role is based in Novara. The role involves identifying potential participants, engaging referral sources, coordinating prescreening, assisting with completing patient procedures during study visits and ensuring compliance with protocol, GDPR, and site SOPs.

Role Type: Onsite

Location: Novara, Italy

Contract Type: Independent Contractor / Freelance

Duration: 6 months with potential for extension

Hours: 20 hours per week

Total Project Hours: 520

Reports To: PI or Designee

Key Responsibilities Prescreening & Recruitment:

Search EMR for potential participants

Coordinate and contact referral sources

Review patient charts/EMRs for eligibility

Review patient lists

Send appointment reminders

Organize and assist with transportation and follow‐up

Patient Visits and Procedures

Vital signs

Blood draws

Documentation & Systems:

Enter data into EDC

Review and QC data in EDC

Maintain accurate and compliant documentation per site, sponsor, and hospital SOPs





Compliance & Training Complete onboarding requirements: training on protocol and study‐related tools and systems, site training including SOPs and workflow

Ensure GDPR‐compliant data handling, including consent for background checks and data usage

EU work authorization and freelancer eligibility (tax ID, self‐employment registration)

GCP certification within the past 2 years required

Criminal record certificate (national) required

Valid professional license/registration in Italy

Qualifications &

Requirements Licensed, university‐educated nurse

Minimum 2 years'

experience as a research nurse and experience as a clinical research coordinator

Demonstrated prescreening / recruitment experience, preferably in metabolic / liver studies

Proficiency with EMRs, EDC, and clinical trial systems

Prior experience with industry‐sponsored trials, strongly desired

Strong attention to detail, independent work ethic, and excellent communication skills

Fluent in Italian and conversational in English; proof of proficiency may be required

Currently live and able to commute to a site located in Novara, Italy

Seniority Level Mid‐Senior level

Employment Type Contract

Job Function Health Care Provider

📌 Research Nurse/Clinical Research Coordinator (Part-time, On-site, Independent Contractor) Nov[...] (Novara)
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