Experteer Overview

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In this role you will provide medical, scientific, and strategic leadership for planning, execution, and reporting of clinical trials. You will act as Medpace’s internal medical expert for review, presentation, and interpretation of results in Clinical Study Reports. You will contribute to the development of new clinical projects, including study design and protocols, across multiple therapeutic areas. This position offers hybrid WFH flexibility and the chance to shape trial design, safety management, and regulatory documents within a collaborative, learning-driven environment.

Compensaciones / Ventajas
• Provide medical management and expertise for clinical trials
• Contribute medical insights to study reports, regulatory documents, and manuscripts




• Manage safety issues in trials and collaborate with associates on evaluation and assessment
• Participate in new business development through proposals and sponsor meetings
• Coordinate with departments across all study phases (feasibility, design, medical information)
• Lead adherence to study protocols and policy requirements

Responsabilidades
• MD degree or equivalent
• Board certification and current medical xqbhyrx licensure preferred
• Prior clinical trial research experience
• Previous experience in pharmaceutical-related clinical research preferred

Requisitos principales
• hybrid WFH flexibility
• competitive compensation
• health, wellness, retirement, and PTO benefits
• on-site mentoring and career development
• industry onboarding and training programs
• dynamic, collaborative culture

📌 Clinical Research Physician (Madrid)
🏢 Medpace
📍 Madrid