Clinical Research Associate, Sponsor Dedicated
Pubblicato il 13-08-2026 - Iqvia in Milano
Experienced Clinical Research Associate, ItalyYour responsibilities will include:Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutionsCollaborating with experts at study sites and with client representativesQualifications:University Bachelor's Degree and Master's Degree in scientific discipline or health careIn possession of CRA Certification as required by Ministerial Decree dated 15.11.2011Experience in Pharma Industry, and/or Clinical Trials environmentVery good computer skills including MS OfficeExcellent command of English languageOrganizational, time management and problem-solving skillsAbility to establish and maintain effective working relationships with coworkers, managers,
and clientsFlexibility to travelDriver's license class BWhat you can expect: Resources that promote your career growthLeaders that support flexible work schedulesPrograms to help you build your therapeutic knowledgeExcellent working environment in a affidabile, international, reputable companyCompany car, mobile phone and attractive benefits packageIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false stat