Experteer Overview In this role you will provide medical, scientific, and strategic leadership for planning, executing, and reporting clinical trials. You will act as Medpace's internal medical expert, guiding interpretation of results in study reports and regulatory documents. You will help shape new clinical projects, including study design and protocols, across multiple therapeutic areas. This position offers hybrid WFH flexibility and an opportunity to impact trials across oncology, neurology, psychiatry, hepatology, dermatology, and metabolic diseases. Retribuzione / Benefits Provide medical management and expertise for clinical trials Contribute medical input to study reports, regulatory documents,



and manuscripts Manage safety issues in clinical trials and collaborate on evaluation of trials Participate in new business development through proposal and sponsor meetings Coordinate with other departments across all study phases (feasibility, design, medical information, and document review) Lead adherence to research-related protocols and policies Responsabilità MD degree or equivalent Board certification and current medical licensure preferred Prior clinical trial research experience Previous experience in pharmaceutical-related clinical research preferred 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

📌 Pharmaceutical physician (Italia)
🏢 Experteer Italy
📍 Italia