Clinical Trial Manager - Italy - Neuroscience / Ophthalmology

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