Clinical Research Associate

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ph3Job Summary /h3 pThe Clinical Research Associate position at Medpace offers 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 pFor those with a medical and/or health/life science background who 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 you! Our successful Clinical Research Associates possess various backgrounds in medical and other science‑related healthcare fields. /p pBackgrounds 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 Assistants MEDPACE CRA TRAINING PROGRAM (PACE) /p pNo research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence: 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 process. /p h3Why BECOME A CRA /h3 pThis 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: /p 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 1,5br/- 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; /li liFamiliarity 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) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. /p pOur mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. /p pWe leverage in‑country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti‑viral and anti‑infective. /p pHeadquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. /p h3Why Medpace? /h3 pWhen you join Medpace, you become part of an innovative team that brings cutting‑edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross‑functional collaboration. /p h3Purpose‑Driven Work /h3 pWork alongside physicians, scientists, and industry‑leading experts committed to advancing the global development of medical therapeutics through clinical research excellence. /p h3Collaborative Culture /h3 pContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. /p h3Leadership throughout Medpace is both accessible and approachable /h3 pContinuous Growth Development /p h3Office based environment with on‑site mentors /h3 pDefined career paths with clear advancement opportunities /p h3Industry renowned onboarding and training programs designed to accelerate professional development /h3 pOngoing training and continuous learning opportunities throughout your career /p pAn environment that encourages employees to influence change, contribute ideas, and grow quickly /p h3Other Employee Benefits /h3 ul liCompetitive compensation programs that recognize and reward performance /li liComprehensive health, wellness, retirement, and PTO benefits /li liOffice based culture with occasional WFH that provides flexibility for eligible positions after training /li liCompany-sponsored social events Please note benefits may vary based on country. /li /ul /p #J-18808-Ljbffr

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