06 sep
|
Medpace
|
Madrid
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 updatesResponsabilidades - 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 applicationsRequisitos 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