Overview In this role you support and expand a network of clinical sites in Europe, focusing on feasibility, site selection, and study start-up. You will partner with cross-functional teams to optimize site performance and intelligence, driving efficient feasibility processes and strong site relationships. You will work in a fast-paced, mission-driven environment that values collaboration and impact.

Retribuzione / Benefits Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Provide ongoing site support and identify future business opportunities and feasibility assessments Develop plans for site contact, follow-up, and relationship management within assigned country Support management in expediting feasibility, site selection and study start-up Serve as site relations and excellence partner,



maintaining relationships with preferred site networks and flagship sites Maintain relationships with network directors, facilitate master CDAs and organize network meetings Support process improvement initiatives for feasibility activities and site performance Serve as main contact for project teams regarding site performance updates and information May be assigned additional projects and responsibilities as needed Bachelor of Science in health-related field Minimum 1 year of site and clinical trials experience CRA experience is an asset Knowledge of drug development, clinical trial management and GCP preferred Knowledge of medical terminology and clinical patient management preferred Fluency in English Proficient in Microsoft Office applications Microsoft Office applications GCP knowledge (preferred) Clinical trials operations familiarity

📌 Coordinator (m/w/d) Projects (Milano)
🏢 Medpace
📍 Milano