Experteer Overview As 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 / Benefits Manage day-to-day project operations per contract and ICH/GCP rules Serve as primary Sponsor contact for operational issues and study deliverables Maintain deep knowledge of protocol, therapeutic area, and indication Oversee internal project team deliverables and provide necessary training Review input for study protocol, edit check specs, data analysis plan,



and final report Develop operational project plans Manage risk assessment and execution Oversee study vendors Manage site quality and supervise CRAs and monitoring deliverables Responsabilità Bachelor's degree in health or life sciences; advanced degree preferred Experience in Phases 1-4 (Phases 2-3 preferred) Minimum 2 years of Clinical Trial Management experience; CRO experience preferred Experience overseeing project timelines Bid defense experience preferred Strong leadership skills Requisiti fondamentali Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives #J-18808-Ljbffr

📌 Clinical trial manager (Italia)
🏢 Experteer Italy
📍 Italia