Experteer Overview
As a CRA Manager in Madrid, you will lead and develop the Clinical Research Associates within the Clinical Monitoring team, ensuring study delivery and CRA performance. You will guide resourcing, training, and oversight to maintain high-quality monitoring and regulatory compliance. This role collaborates with CTMs and cross-functional partners to meet project objectives and drive continuous improvement. You will influence CRA retention and act as a key resource for issue resolution, shaping the team’s effectiveness and growth.

Compensaciones / Incentivos
• Line management of Clinical Research Associates (CRAs)
• Recruitment of CRAs
• Training and development of CRAs in collaboration with Training u0026 Development
• Oversight of CRA performance and adherence to standards
• Tracking CRA resourcing and allocating studies
• Managing turnover and retention of CRAs




• Support CTMs to achieve project objectives related to CRA performance and compliance
• May serve as lead CRA as needed

Responsabilidades
• Life Science Bachelor's degree
• At least 4 years' CRA experience in the specified country
• Minimum 2-3 years of experience as CRAM
• Advanced knowledge of Good Clinical Practice and Local Regulations
• Strong leadership, mentoring, and motivational skills
• Effective written and verbal communication skills
• Proficient in Microsoft Office
• Fluent in English and Spanish
• Office-based in Madrid, Spain
• Occasional travel (10-20%)

Requisitos principales
• Competitive compensation
• Comprehensive health, wellness, retirement, and PTO benefits
• Office-based culture with occasional WFH
• Company-sponsored social events

📌 Clinical Research Associate (CRA) Manager (Madrid)
🏢 Medpace
📍 Madrid