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
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📌 Pharmaceutical Physician (Italia)
🏢 Altro
📍 Italia