Clinical Research Associate

Join to apply for theClinical Research Associaterole atMedpace Continue with Google Continue with Google Join to apply for theClinical Research Associaterole atMedpace 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 youOur successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields. Backgrounds of individuals who have succeeded in the CRA role include:Nursing Dietetics Pharmacist Pharmaceutical/Device Sales Representative Biomedical/Chemical Engineer PhD/Post-Doc Pharm.D candidate Health and Wellness Coordinators Clinical Research Coordinators Research AssistantsMEDPACE CRA TRAINING PROGRAM ( PACE )No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through ourPACETraining Program, you will join otherP rofessionalsA chievingC RAE xcellence: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 CRA PACE will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums To 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 CRAThis role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:Dynamic working environment, with varying responsibilities day-to-day Expansive experience in multiple therapeutic areas Work within a team of therapeutic and regulatory experts Defined CRA promotion and growth ladder with potential for mentoring and management advancements Competitive pay. Bonus for CRA with 1,5 - 5 years of monitoring experience.ResponsibilitiesConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical 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; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.QualificationsMaster degree in health-related field; Willing to travel 60-80% nationally; Familiarity with Microsoft Office; CRA certification completed as per DMC 15 /11 / 2011; Fluent in English and Italian language; Strong communication and presentation skills a plus.Medpace 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 environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiativesAwardsRecognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 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. Seniority levelSeniority level Not Applicable Employment typeEmployment type Full-time Job functionJob function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Medpace by 2x Sign in to set job alerts for “Clinical Research Associate” roles.Continue with Google Continue with Google Continue with Google Continue with Google Clinical Project Coordinator - Entry LevelClinical Research Associate, Site Management - ItalyClinical Research Associate (CRA) - Law 68/99 Art. 18Experienced Clinical Research Associate (CRA)CRA II/Sr CRA - HOME BASED ROME (MANDATORY)Clinical Research Associate, Site Management - ItalyClinical Research Associate, Sponsor Dedicated - ItalyAssociate Clinical Trial Manager (PhD) - Infectious Disease / ImmunologyCRA II/Sr CRA - HOME BASED ROME (MANDATORY)Associate Clinical Trial Manager (PhD) - Neuroscience / OphthalmologyExperienced CRA, Sponsor Dedicated - Italy(Associate) Medical Director - NeurologyWe’re unlocking community knowledge in a new way. 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