Experteer Overview 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 / Ventajas • 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, 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