The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development.For those with medical and/or health/life science interest and background who want to explore the research field,and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you! Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. PACE – MEDPACE CRA TRAINING PROGRAM No clinical experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.

Through our PACE Training Program, you will join other P rofessionals A chieving C RA E xcellence: To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process. This rolewill allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. Conduction of qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol

- Communication with the medical site staff including coordinators, clinical research physicians and their site staff
- Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
- Medical record and research source documentation verification against case report form data,



including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements
- Regulatory document review
- Medical device and/or investigational product/drug accountability and inventory
- Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
- Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement
- Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. Must have a minimum of a university degree in a health or life science related field
- Proficient knowledge of Microsoft® Office and general computer literacy
- Excellent verbal and written communication skills in English and Spanish 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. 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. Work alongside physicians, scientists, and industry-leading experts committed to advancing the general development of medical therapeutics through clinical research excellence Office based environment with on-site mentors Industry renowned onboarding and training programs designed to accelerate professional development Ongoing training and continuous learning opportunities throughout your career 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

📌 German speaking CRA (Madrid)
🏢 Medpace
📍 Madrid