Clinical Research Associate Job at Medpace, Spain | Life Science | Apply Now
Are you looking to transition your scientific knowledge into a dynamic, field-based role that brings life-saving treatments to market? Medpace is offering a unique opportunity to launch a rewarding Life Sciences Career right from Madrid, Spain. Through their industry-renowned entry-level training initiative, this Junior Clinical Research Associate Job requires no prior clinical monitoring experience. It is the perfect gateway for motivated graduates and healthcare professionals looking to secure an impactful, long-term Medpace career.
- Job Position: Junior Clinical Research Associate
- Location:Â Madrid, Spain
- Category: Clinical Research Associate
- Job ID:Â 12067
About The Company
Medpace is a scientifically driven, full-service clinical Contract Research Organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs more than 6,000 people across 40+ countries. The company leverages deep local regulatory and medical expertise across major high-stakes areas, including oncology, cardiology, metabolic disease, endocrinology, the central nervous system, and anti-infectives. Medpace was recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024) and continually wins CRO Leadership Awards for quality, expertise, and reliability.
The PACE CRA Training Program
The standout feature of starting your Medpace career as a junior monitor is the platform’s comprehensive, unmatched onboarding framework. Through the PACE (Professionals Achieving CRA Excellence) training program, Medpace bridges the gap for those new to clinical trials.
- Foundational Platform: PACE provides the exact tools and interactive discussions needed to effectively and confidently carry out independent field monitoring.
- Practical Learning: The curriculum develops your skills through hands-on, job-related exercises, case-study practicums, and interactive clinical simulations.
- Core Rotations: To supplement your field-based training, you will participate in multi-departmental clinical research core rotations, gaining an all-encompassing understanding of the global drug and device approval process.
Clinical Research Associate Job – Key Responsibilities
As an independent monitor, you will serve as the primary operational link between Medpace project teams and clinical trial sites across the region.
Your day-to-day responsibilities in this Clinical Research Associate Job will include:
- Site Lifecycle Visits: Conducting routine qualification, initiation, monitoring, and closeout visits for research sites in absolute compliance with the approved protocol and Good Clinical Practice (GCP).
- Source Data Verification: Reviewing medical records and research source documentation against electronic case report forms (CRFs) to identify entry errors and enforce good documentation practices.
- Compliance & Deviations: Verifying investigator qualifications, checking site equipment/laboratories, ensuring only eligible subjects are enrolled, and communicating protocol deviations per SOPs.
- Investigational Product Accountability: Managing and tracking medical device or investigational drug inventories, accountability logs, and storage conditions at the site level.
- Safety Review: Reviewing and verifying adverse events (AEs), serious adverse events (SAEs), and concomitant medications to confirm accurate safety reporting.
- Site Metrics & Reporting: Assessing patient recruitment or retention success, offering proactive suggestions for improvement, and compiling detailed monitoring reports and follow-up letters to secure site compliance.
Qualifications Required For Clinical Research Associate Job
Medpace welcomes applicants from varied backgrounds in medical and other science-related healthcare fields who possess a strong desire to learn.
- Educational Foundation: Must have a minimum of a university degree in a health or life science-related field.
- Linguistic Mastery: Excellent verbal and written communication skills in both English and Spanish are strictly required. Please note that your application must be submitted in English.
- Mobility Readiness: Willingness and ability to maintain approximately 60–80% travel to clinical sites.
- Core Professional Competencies: Outstanding presentation skills, a detail-oriented mindset, efficient time management, and general computer literacy with proficiency in the Microsoft Office suite.
Stepping into a Clinical Research Associate Job with Medpace means enjoying a varied daily routine alongside highly structured corporate perks. In summary, this Junior CRA position is a definitive launchpad for any ambitious life sciences graduate in Spain. By bypassing the usual requirement for prior monitoring experience via the PACE training program, Medpace allows you to dive straight into high-stakes clinical operations. If you possess the required bilingual skills, an analytical mind, and a passion for medical innovation, apply today to secure this premier position and kickstart a lifelong Life Sciences Career.
