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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, pre
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