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

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