Experteer OverviewAs a Clinical Trial Manager at Medpace in Milan, you lead day-to-day project operations for CNS/Neuroscience studies, collaborating with cross-functional teams to meet study milestones and regulatory requirements. You act as the main Sponsor contact for operational issues and ensure high-quality deliverables. You’ll shape protocols and operational plans while managing risks, vendors, and site quality to help accelerate therapeutic development.Retribuzione / BenefitsManage day-to-day project operations per contract and ICH/GCP rulesServe as primary Sponsor contact for operational issues and study deliverablesMaintain deep knowledge of protocol, therapeutic area, and indicationOversee internal project team deliverables and provide necessary trainingReview input for study protocol, edit check specs, data analysis plan, and final reportDevelop operational project plansManage risk assessment and executionOversee study vendorsManage site quality and supervise CRAs and monitoring deliverablesResponsabilitàBachelor's degree in health or life sciences; advanced degree preferredExperience in Phases 1-4 (Phases 2-3 preferred)Minimum 2 years of Clinical Trial Management experience; CRO experience preferredExperience overseeing project timelinesBid defense experience preferredStrong leadership skillsRequisiti fondamentaliFlexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiatives
#J-18808-Ljbffr