Overview
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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 global CRO. You will contribute to compliant, high-quality study conduct with potential for mentoring and leadership opportunities.
Compensaciones / Beneficios
Adaptable 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 xhfqzwm 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
📍 Barcelona