Job Summary
Medpaceis growing quickly, and we are seeking anoffice-based Clinical Research Associate (CRA) Managerto join our Clinical Monitoring team inMadrid. The CRA Manager plays a key role in the clinical trial management process atMedpace. If you want an exciting career where you use yourpreviousCRAexpertiseand 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 withTraining&Developmentdepartment;
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 objectivesin regards toCRA performance standards, monitoringconsistencyand compliance;alsoin trouble shooting and serve as a resource for issue resolution
May serve as a lead CRA as needed
Qualifications
Life ScienceBachelor’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 skills
Proficient knowledge of Microsoft® Office software
Fluent in Englishand Spanish
This position is office based inMadrid,Spain
Occasionaltravel(10-20%)
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic,



endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work

Work alongside physicians, scientists, and industry-leading experts committed to advancing the integral development of medical therapeutics through clinical research excellence

Collaborative Culture

Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

Office based environment with on-site mentors
Defined career paths with clear advancement opportunities
Industry renowned onboarding and training programs designed to accelerate professional development
Ongoing training and continuous learning opportunities throughout your career
An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

Competitive compensation programs that recognize and reward performance
Comprehensive health, wellness, retirement, and PTO benefits
Office based culture with occasional WFH that provides flexibility for eligible positions after training
Company-sponsored social events

Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
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📌 Clinical Research Associate (CRA) Manager (Madrid)
🏢 Medpace
📍 Madrid