ppOur clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. /ppMedpace will provide comprehensive initial and ongoing training depending on your previous experience. /ph3Responsibilities /h3ulliConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; /liliCommunication with the medical site staff including coordinators, clinical research physicians, and their site staff; /liliVerify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; /liliMedical 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; /liliVerification that the investigator is enrolling only eligible subjects; /liliRegulatory document review; /liliMedical device and/or investigational product/drug accountability and inventory; /liliVerification and review of adverse events, serious adverse events,



concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; /liliAssess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and /liliCompletion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. /li /ulh3Qualifications /h3ulliMaster degree in health-related field; /liliCRA certification completed as per DMC 15 /11 / 2011; /liliPrevious experience as CRA; /liliWilling to travel up to 60-80% nationally; /liliFamiliarity with Microsoft® Office; /liliFluent in English and Italian language; /liliStrong communication and presentation skills would be considered as a plus. /li /ulh3Compensation /h3pEUR €43,000.00/Yr. - EUR €76,000.00/Yr. /ph3Medpace Overview /h3pMedpace 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 6,000 people across 40+ countries. /ph3Why Medpace? /h3pPeople. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. /ppThe work we’ve done over the past 30+ years has positively impacted 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. /ph3Medpace Perks /h3ulliFlexible work environment /liliCompetitive compensation and benefits package /liliCompetitive PTO packages /liliStructured career paths with opportunities for professional growth /liliCompany-sponsored employee appreciation events /liliEmployee health and wellness initiatives /li /ulh3Awards /h3ulliRecognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 /liliContinually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility /li /ulh3What To Expect Next /h3pA 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 (CRA) (Italia)
🏢 Medpace
📍 Italia