Overview In this full-time, home-based CRA role in Barcelona, you support patients and sites as Medpace accelerates the development of pharmaceuticals and medical devices. You join a training-focused program (PACE) to build independent CRA expertise through hands-on practice and rotations. The role offers diverse therapeutic exposure, cross-functional collaboration, and clear growth paths within a general CRO. You will contribute to compliant, high-quality study conduct with potential for mentoring and leadership opportunities.

Compensaciones / Beneficios

Flexible work environment Competitive compensation and benefits package Competitive PTO Structured career paths with growth Company-sponsored employee appreciation events Employee health and wellness initiatives

Responsabilidades

Conduct qualification, initiation, monitoring, and closeout visits per protocol Communicate with site staff including coordinators and investigators Verify investigator qualifications, training, resources, and facilities Verify data accuracy and ensure Good Documentation Practices; address protocol deviations per SOPs, GCP,



and regulatory requirements Ensure enrollment of eligible subjects and perform regulatory document reviews Oversee medical device/investigational product/drug accountability Review adverse events and concomitant medications for accurate reporting Assess site recruitment/retention and suggest improvements Complete monitoring reports and follow-up letters with actionable recommendations to ensure compliance

Requisitos principales

University degree in a health or life science related field Minimum 1 year experience as Study Coordinator (SC), CRC, or CRA trainee Approximately 60-80% travel Proficient Microsoft Office and general computer literacy Outstanding communication and presentation skills Detail-oriented with good time management Excellent verbal and written communication in English and Spanish Catalan language fluency is a plus strong communication attention to detail time management Microsoft Office Good Documentation Practices (GDP) GCP compliance

📌 Clinical Research Associate - Barcelona - Medpace
🏢 Medpace
📍 Barcelona