Descripción del trabajo 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 / Beneficios
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
versátil work arrangements after training

📌 German speaking CRA (Madrid)
🏢 Medpace
📍 Madrid