Overview In this role you will manage day-to-day clinical trial operations and serve as the primary sponsor contact. You’ll apply your CNS/Neuroscience expertise or broaden to other areas while ensuring compliance with ICH/GCP and regulatory standards. You’ll lead cross-functional teams, oversee vendors and sites, and contribute to protocol and study deliverables. This position sits in Medpace’s Clinical Trial Management Group in Milan, offering flexibility after probation and a strong focus on impact through global trial execution. Retribuzione / Benefits * 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 Responsabilità * Oversee day-to-day trial operations per contract and regulatory requirements * Act as primary Sponsor contact for operational issues and study deliverables * Maintain deep knowledge of protocol, therapeutic area, and indication * Provide cross-functional oversight and ensure training for project team members * Review and provide input on protocol, edit check specs, and data analysis plans * Develop operational project plans and manage risk and vendor relationships * Supervise site quality and monitor deliverables by Clinical Research Associates Requisiti fondamentali * Bachelor’s degree in a health or life science-related field * Minimum 2 years of Clinical Trial Management experience * CRO experience preferred * Experience in Phases 1-4 (Phases 2-3 preferred) * Management of overall project timeline * Strong leadership skills * Bid defense experience preferred * leadership * cross-functional collaboration * problem solving * ICH/GCP knowledge * study protocol review * data analysis plan input

📌 Clinical Trial Manager (Monza)
🏢 Medpace
📍 Monza