Clinical Research Associate

ppThe Clinical Research Associate position at Medpace offers the unique opportunity to have an bexciting career /b in the research of drug and medical device development while bmaking a difference /b in the lives of those around them. For those with a bmedical and/or health/life science background /b who want to explore the research field and be part of a team bringing pharmaceutical and medical devices to market—bthis could be the right opportunity for you! /b /p h3Backgrounds of Successful CRAs /h3 ul liNursing /li liDietetics /li liPharmacist /li liPharmaceutical/Device Sales Representative /li liBiomedical/Chemical Engineer /li liPhD/Post-Doc /li liPharm.D candidate /li liHealth and Wellness Coordinators /li liClinical Research Coordinators /li liResearch Assistants /li /ul h3MEDPACE CRA TRAINING PROGRAM (PACE) /h3 ul liPACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA /li liPACE will prepare you by developing your CRA skills through interactive discussions and hands‑on job‑related exercises and practicums /li liTo 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 /li /ul h3WHY BECOME A CRA /h3 ul liDynamic working environment, with varying responsibilities day‑to‑day /li liExpansive experience in multiple therapeutic areas /li liWork within a team of therapeutic and regulatory experts /li liDefined CRA promotion and growth ladder with potential for mentoring and management advancements /li liCompetitive pay /li liBonus for CRA with 1.5-5 years of monitoring experience /li /ul h3Responsibilities /h3 ul liConduct qualification, initiation, monitoring, and closeout visits at 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 liVerify 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 liAssess 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 liMaster degree in health‑related field /li liWilling to travel 60-80% nationally /liliFamiliarity with Microsoft® Office /li liCRA certification completed as per DMC 15/11/2011 /li liFluent in English and Italian language /li liStrong communication and presentation skills a plus /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. The 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. /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