Ph3Experteer Overview /h3pAs 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. /ph3Retribuzione / Benefits /h3ulliManage day-to-day project operations per contract and ICH/GCP rules /liliServe as primary Sponsor contact for operational issues and study deliverables /liliMaintain deep knowledge of protocol, therapeutic area, and indication /liliOversee internal project team deliverables and provide necessary training /liliReview input for study protocol, edit check specs, data analysis plan, and final report /liliDevelop operational project plans /liliManage risk assessment and execution /liliOversee study vendors /liliManage site quality and supervise CRAs and monitoring deliverables /li /ulh3Responsabilità /h3ulliBachelor's degree in health or life sciences; advanced degree preferred /liliExperience in Phases 1-4 (Phases 2-3 preferred) /liliMinimum 2 years of Clinical Trial Management experience; CRO experience preferred /liliExperience overseeing project timelines /liliBid defense experience preferred /liliStrong leadership skills /li /ulh3Requisiti fondamentali /h3ulliFlexible work environment /liliCompetitive compensation and benefits package /liliCompetitive PTO packages /liliStructured career paths with opportunities for professional growth /liliCompany-sponsored employee appreciation eventsEmployee health and wellness initiatives /li /ul /p #J-18808-Ljbffr