Experteer Overview
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In this role you will strengthen and manage relationships with clinical sites across Spain, driving feasibility assessments and pre/post-award strategies to accelerate study start-up. You’ll work closely with the Clinical Operations team to identify new business opportunities and optimize site performance. You will help build a knowledgeable site network, support site selection, and improve feasibility processes to deliver high-quality trials. This is a growth-focused position within a dynamic CRO that values collaboration and impact.
Compensaciones / Beneficios
• Support site relations and explore future business opportunities and feasibility assessments
• Create and execute plans for site contact, contact follow-up, and issue resolution
• Assist management with feasibility, site selection, and study start-up activities
• Maintain oversight of assigned sites and build relationships within the country
• Conduct/expedite feasibility activities and align sites with studies/therapeutic areas
• Research site landscape including KOLs, site capabilities, and country practices relevant to patient populations




• Develop and maintain a network of preferred sites and facilitate master CDAs
• Perform regular site performance reviews to ensure quality study delivery
• Act as escalation point for site-related issues across the study lifecycle
• Prepare for site audits and support qualification visits as needed
• Contribute to process improvements in feasibility activities
• Serve as main contact for project teams regarding site performance and updates
• Other projects as assigned
Responsabilidades
• Bachelor of Science in health-related field (minimum)
• Minimum 1 year of site and clinical trials experience
• CRA experience is an asset
• Knowledge of drug development, clinical xqbhyrx trial management 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
• Versátil 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

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