Research Nurse/Clinical Research Coordinator (Part-Time, On-Site, Independent Contractor) Nov[...] (Novara)

Research Nurse/Clinical Research Coordinator (Part-Time, On-Site, Independent Contractor) Nov[...] (Novara)

18 giu
|
RapidTrials
|
Novara

18 giu

RapidTrials

Novara

Research Nurse/Clinical Research Coordinator (Part-time, On-site, Independent Contractor) Novara ItalyRapidTrials 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. Non aspetti a candidarsi dopo aver letto questa descrizione: per questa opportunità è previsto un elevato volume di candidature. This tempo parziale, 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: OnsiteLocation: Novara, ItalyContract Type: Independent Contractor / FreelanceDuration: 6 months with potential for extensionHours: 20 hours per weekTotal Project Hours: 520Reports To: PI or DesigneeKey ResponsibilitiesPrescreening & Recruitment:Search EMR for potential participantsCoordinate and contact referral sourcesReview patient charts/EMRs for eligibilityReview patient listsSend appointment remindersOrganize and assist with transportation and follow-upPatient Visits and Procedures:Vital signsBlood drawsDocumentation & Systems:Enter data into EDCReview and QC data in EDCMaintain accurate and compliant documentation per site, sponsor, and hospital SOPsCompliance & TrainingComplete onboarding requirements: training on protocol and study-related tools and systems, site training including SOPs and workflowEnsure GDPR-compliant data handling, including consent for background checks and data usageEU work authorization and freelancer eligibility (tax ID, self-employment registration)GCP certification within the past 2 years requiredCriminal record certificate (national) requiredValid professional license/registration in ItalyQualifications & RequirementsLicensed, university-educated nurseMinimum 2 years' experience as xrdztoy a research nurse and experience as a clinical research coordinatorDemonstrated prescreening / recruitment experience, preferably in metabolic / liver studiesProficiency with EMRs, EDC, and clinical trial systemsPrior experience with industry-sponsored trials, strongly desiredStrong attention to detail, independent work ethic, and excellent communication skillsFluent in Italian and conversational in English; proof of proficiency may be requiredCurrently live and able to commute to a site located in Novara, ItalySeniority LevelMid-Senior levelEmployment TypeContractJob FunctionHealth Care Provider #J-*****-Ljbffr

📌 Research Nurse/Clinical Research Coordinator (Part-Time, On-Site, Independent Contractor) Nov[...] (Novara)
🏢 RapidTrials
📍 Novara

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