CRA - MONITOR
Pubblicato il 01-08-2026 - Altro in Italia
OverviewIn this role, you will support multinational clinical studies by coordinating site activities and ensuring high-quality data. Sia tra i primi a candidarsi: legga la panoramica completa del ruolo qui sotto, quindi invii la sua candidatura per essere preso/a in considerazione. You will work within a cross‐functional team to monitor sites, manage regulatory submissions, and help optimize recruitment. You'll contribute to compliant trial conduct aligned with GCP and ICH standards, impacting patient outcomes and study success. This is an international, growth‐oriented opportunity with strong support for professional development and a stable, reputable employer.ResponsibilitiesPerform site selection, initiation, monitoring and close‐out visitsSupport development of a subject recruitment planEvaluate quality and integrity of site practices per GCP/ICHManage progress by tracking regulatory submissions, recruitment, CRF completion,
and data query resolutionsCollaborate with study site experts and client representativesBachelor's Degree and Master's Degree in a scientific discipline or health careCRA Certification as required by Ministerial Decree dated 15.11.2011Experience in Pharma Industry and/or Clinical TrialsVery good computer skills including MS OfficeExcellent xrdztoy command of EnglishStrong organizational, time management and problem‐solving skillsAbility to establish and maintain effective working relationships with coworkers, managers, and clientsFlexibility to travelDriver's license class BBenefitsCareer growth resourcesFlexible work schedulesTherapeutic knowledge programsCompany carMobile phoneAttractive benefits package #J-18808-Ljbffr