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
📍 Barcelona