ph3Overview /h3 pThe Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. /p pbWhat can Medpace offer you? /b /p ul liInteresting projects, career advancement, and recognition and exposure to our international footprint; /li liFlexible working conditions - Opportunity to work from home and versátil working hours; /li liCompetitive employee benefits; /li liAnnual Merit increases; /li liFast PACE® - Accelerated, tailored training program based on your experience; /li liOpportunity for cross-functional and CRA leadership positions - Lead CRA, CRA Manager, Clinical Trial Manager; /li liSign on bonus may be appropriate for qualifying candidates. /li /ul h3Responsibilities /h3 ul liConduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol; /li liCommunication with the medical site staff including coordinators, clinical research physicians and their site staff; /li liVerifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; /li liMedical 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; /li liVerification that the investigator is enrolling only eligible subjects; /li liRegulatory document review; /li liMedical device and/or investigational product/drug accountability and inventory; /li liVerification and review of adverse events,



serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; /li liAssessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; /li liCompletion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. /li /ul h3Qualifications /h3 ul liMust have a minimum of a university degree in a health or life science related field; /li li1.5 years’ work experience as a CRA; /li liOncology monitoring experience would be an advantage; /li liWilling to travel approximately 60-80% nationally; /li liFamiliarity with Microsoft® Office; /li liMust be detail-oriented and efficient in time management; /li liStrong communication and presentation skills a plus; /li liProven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities. /li liExcellent verbal - written communication skills and excellent negotiations skills in Spanish and English. /li liExcellent time management and organization skills. /li /ul h3Medpace Overview /h3 pMedpace is a full-service clinical contract research organization (CRO).



We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. /p h3Why Medpace? /h3 pPeople. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. /p pThe work we’ve done over the past 30+ years has positively impact the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. /p h3Medpace Perks /h3 ul liFlexible work environment /li liCompetitive compensation and benefits package /li liCompetitive PTO packages /li liStructured career paths with opportunities for professional growth /li liCompany-sponsored employee appreciation events /li liEmployee health and wellness initiatives /li /ul h3Awards /h3 ul liRecognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 /li liContinually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility /li /ul h3What To Expect Next /h3 pA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. /p /p #J-18808-Ljbffr

📌 Experienced Clinical Research Associate (Barcelona)
🏢 Medpace
📍 Barcelona