Experteer Overview
As a Clinical Research Associate at Medpace, you contribute to the development of pharmaceuticals and medical devices by supporting site management and data integrity. You join a collaborative team that emphasizes training, growth, and cross-functional exposure across therapeutic areas. You will engage in site qualification, monitoring, and regulatory activities that ensure compliant, high-quality trials. This role offers a clear path for advancement within a purpose-driven, globally active organization.

Compensaciones / Ventajas
• Conduct qualification, initiation, monitoring, and closeout visits in line with the protocol
• Communicate with site staff including coordinators and physicians
• Verify investigator qualifications, training, facilities, and resources
• Verify medical records and source data against case report forms and ensure adherence to GCP and SOPs
• Ensure enrolling only eligible subjects and perform regulatory document reviews




• Manage device/investigational product/drug accountability and inventory
• Review adverse events and related data for accuracy and compliance
• Assess site recruitment/retention and suggest improvements
• Prepare monitoring reports and follow-up letters with notable findings and recommended actions

Responsabilidades
• Minimum university degree in a health or life science related field
• Approximately 60-80% travel
• Proficient Microsoft Office and general computer literacy
• Outstanding communication and presentation skills
• Detail-oriented with strong time management
• Excellent verbal and written communication in English and Spanish
• Application submitted in English

Requisitos principales
• competitive pay
• comprehensive health benefits
• retirement benefits
• PTO
• on-site mentorship and training
• flexible work arrangements after training

📌 Junior Clinical Research Associate (Madrid)
🏢 Medpace
📍 Madrid