Experteer OverviewAs an experienced Clinical Research Associate, you will oversee site activities across the trial lifecycle to ensure regulatory compliance and data integrity.
You will work with study sites and client representatives to meet recruitment and submission milestones, while maintaining high-quality practices in line with GCP and ICH guidelines.
This role combines hands?on site monitoring with cross?functional coordination to drive trial success.
Join a reputable, international environment that supports career growth and flexible work arrangements.Retribuzione / BenefitsPerform site selection, initiation, monitoring and close?out visitsSupport the development of a subject recruitment planEvaluate site practices for quality and regulatory compliance (GCP/ICH)Manage progress by tracking regulatory submissions, recruitment, CRF completion,



and data query resolutionsCollaborate with study site experts and client representativesResponsabilitàBachelor in scientific discipline or health careCRA Certification as required by Ministerial Decree dated **********Experience in Pharma Industry or Clinical TrialsVery good computer skills including MS OfficeExcellent 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 BRequisiti fondamentalicompany carmobile phoneattractive benefits packagecareer growth resourcesflexible work schedules#J-*****-Ljbffr

📌 Clinical Research Associate, Sponsor Dedicated - Italy (Bardi)
🏢 Experteer Italy
📍 Bardi