Clinical Research Associate (CRA) Manager

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.

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 skills  Proficient knowledge of Microsoft® Office software   Fluent in English and Spanish  This position is office based in Madrid, Spain  Occasional travel (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 global 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