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In this role you will support and strengthen site relationships in Spain, focusing on feasibility activities and pre-/post-award study planning. You work closely with the Clinical Operations team to identify opportunities, optimize site selection, and accelerate study start-up. You will engage a network of sites and flagship partners, helping shape feasibility strategies and site performance. This is a hands-on, cross-functional role that drives site excellence and efficient trial delivery.
Compensaciones / Beneficios
• Provide ongoing site support and identify future business opportunities and feasibility assessments
• Develop plans for site contact, follow-up, and troubleshooting
• Assist management with feasibility, site selection, and study start-up
• Serve as site relations and excellence partner within the country
• Research site landscape and intelligence (KOLs, capabilities, care standards) for patient recruitment and retention
• Manage relationships with site networks/flagship sites, facilitate master CDAs, and liaise with network directors
• Conduct regular site performance reviews to ensure quality study delivery




• Act as escalation point for site-related issues throughout the study life cycle
• Provide ongoing support for site qualification visits and audits as needed
• Develop an intelligence database with site and country insights
• Support process improvements in feasibility activities
• Be main contact for project teams regarding site performance updates
Responsabilidades
• Bachelor of Science in a health-related field
• Minimum 1 year of site and clinical trials experience (more for senior roles)
• CRA experience is an asset
• Knowledge of drug development, clinical trial management, xqbhyrx and GCP preferred
• Knowledge of medical terminology and clinical patient management preferred
• Fluency in English and Spanish
• Strong organizational and prioritization skills
• Excellent oral and written communication skills
• Proficient in Microsoft Office applications
Requisitos principales
• Competitive compensation
• Comprehensive health, wellness, retirement, and PTO benefits
• WFH flexibility after training
• Office-based with on-site mentors
• Defined career paths with advancement opportunities
• Industry onboarding and training programs

📌 Clinical Trial Site Relationship Coordinator (Madrid)
🏢 Medpace
📍 Madrid