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

ph3Research Nurse/Clinical Research Coordinator (Part-time, On-site, Independent Contractor) Novara Italy /h3pRapidTrials 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. /ppbRole Type: /b Onsite /ppbLocation: /b Novara, Italy /ppbContract Type: /b Independent Contractor / Freelance /ppbDuration: /b 6 months with potential for extension /ppbHours: /b 20 hours per week /ppbTotal Project Hours: /b 520 /ppbReports To: /b PI or Designee /ph3Key Responsibilities /h3pbPrescreening Recruitment: /b /pulliSearch EMR for potential participants /liliCoordinate and contact referral sources /liliReview patient charts/EMRs for eligibility /liliReview patient lists /liliSend appointment reminders /liliOrganize and assist with transportation and follow‑up /li /ulpbPatient Visits and Procedures: /b /pulliVital signs /liliBlood draws /li /ulpbDocumentation Systems: /b /pulliEnter data into EDC /liliReview and QC data in EDC /liliMaintain accurate and compliant documentation per site, sponsor, and hospital SOPs /li /ulh3Compliance Training /h3ulliComplete onboarding requirements: training on protocol and study‑related tools and systems, site training including SOPs and workflow /liliEnsure GDPR‑compliant data handling, including consent for background checks and data usage /liliEU work authorization and freelancer eligibility (tax ID, self‑employment registration) /liliGCP certification within the past 2 years required /liliCriminal record certificate (national) required /liliValid professional license/registration in Italy /li /ulh3Qualifications Requirements /h3ulliLicensed, university‑educated nurse /liliMinimum 2 years’ experience as a research nurse and experience as a clinical research coordinator /liliDemonstrated prescreening / recruitment experience, preferably in metabolic / liver studies /liliProficiency with EMRs, EDC, and clinical trial systems /liliPrior experience with industry‑sponsored trials, strongly desired /liliStrong attention to detail, independent work ethic, and excellent communication skills /liliFluent in Italian and conversational in English; proof of proficiency may be required /liliCurrently live and able to commute to a site located in Novara, Italy /li /ulh3Seniority Level /h3pMid‑Senior level /ph3Employment Type /h3pContract /ph3Job Function /h3pHealth Care Provider /p /p #J-18808-Ljbffr