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

📌 Start-Up Coordinator (Italia)
🏢 Medpace
📍 Italia