Clinical Research Associate

The Clinical Research Associate position at Medpace offers the unique opportunity to have anexciting careerin the research of drug and medical device development whilemaking a differencein the lives of those around them.For those with amedical and/or health/life science backgroundwho 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 youBackgrounds of Successful CRAsNursingDieteticsPharmacistPharmaceutical/Device Sales RepresentativeBiomedical/Chemical EngineerPhD/Post-DocPharm.D candidateHealth and Wellness CoordinatorsClinical Research CoordinatorsResearch AssistantsMEDPACE CRA TRAINING PROGRAM (PACE)PACE 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 CRAPACE will prepare you by developing your CRA skills through interactive discussions and hands-on job-related exercises and practicumsTo 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 processWHY BECOME A CRADynamic working environment, with varying responsibilities day-to-dayExpansive experience in multiple therapeutic areasWork within a team of therapeutic and regulatory expertsDefined CRA promotion and growth ladder with potential for mentoring and management advancementsCompetitive payBonus for CRA with 1.5-5 years of monitoring experienceResponsibilitiesConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocolCommunication with the medical site staff including coordinators, clinical research physicians, and their site staffVerify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staffMedical 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 requirementsVerification that the investigator is enrolling only eligible subjectsRegulatory document reviewMedical device and/or investigational product/drug accountability and inventoryVerification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocolAssess the clinical research site's patient recruitment and retention success and offering suggestions for improvementCompletion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure complianceQualificationsMaster degree in health-related fieldWilling to travel *****% nationallyFamiliarity with Microsoft® OfficeCRA certification completed as per DMC 15/11/2011Fluent in English and Italian languageStrong communication and presentation skills a plusMedpace OverviewMedpace 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.Why Medpace?People.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.Medpace PerksFlexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesAwardsRecognized by Forbes as one of America's Most Successful Midsize Companies in ****, ****, **** and ****Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.#J-*****-Ljbffr