Medpace is growing quickly, and we are seeking an office-based Clinical Research Associate (CRA) Manager to join our Clinical Monitoring team in Madrid. The CRA Manager plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous CRA expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

- Line management of Clinical Research Associates (CRAs)
- Recruitment
- Involvement in training and development of the CRAs in collaboration with Training & Development department
- Oversight of CRAs to ensure they meet expectations
- Tracking and management of CRA Resourcing and allocation of studies assignment
- Turnover and retention of CRAs to meet company objectives
- Assist Clinical Trial Managers (CTM) with achieving project objectives in regards to CRA performance standards, monitoring consistency and compliance; also in trouble shooting and serve as a resource for issue resolution




- May serve as a lead CRA as needed

Qualifications

- Life Science Bachelor’s degree
- At least 4 years' experience as CRA in 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 skillsProficient knowledge of Microsoft Office software
- Fluent in English and Spanish
- This position is office based in Madrid, Spain
- Occasional travel (10-20%)

Medpace Perks

- Versátil work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives

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