The Clinical Research Associate at Medpace is offeringthe unique opportunity to have an exciting career in the researchof drug and medical device development while making a difference inthe lives of those around them. For those with medical and/orhealth/life science interest and background who want to explore theresearch field, travel the UK, and be part of a team bringingpharmaceutical and medical devices to market - this could be theright opportunity for you! Please note that to take full advantageof the training on offer, you must be within commuting distance ofour Medpace central London office. Our successful Clinical ResearchAssociates possess varied backgrounds in medical and otherscience-related healthcare fields. Individuals who have succeededin the CRA role include: - Nurses - Dieticians - PharmacyTechnicians - Pharmaceutical/Device Sales Representatives - BiotechEngineers - PhD/Pharm.D candidates - Health and WellnessCoordinators - Site Coordinators, Clinical Research Coordinators -Research Assistants. PACE® - MEDPACE CRA TRAINING PROGRAM Throughour PACE® Training Program, you will join other P rofessionals Achieving C RA E xcellence: - PACE® provides the platform toeffectively and confidently carry out your duties, enhance yourcurrent abilities and ultimately help you become a high-functioningindependent Medpace CRA. - PACE® will prepare you by developingyour CRA skills through interactive discussions and hands onjob-related exercises and practicums. - To supplement your in-houseand field-based training you may also participate in other clinicalresearch departmental core rotations, learning other aspects of thedrug/device development and approval process. UNEXPECTED REWARDSThis role takes you on a journey through travel and excitementwhich will allow you to make a difference on a large scale throughthe enhancement of pharmaceuticals and medical devices. The CRAposition provides many other distinctive advantages including: -Dynamic working environment, with varying responsibilities day-today - Expansive experience in multiple therapeutic areas - Workwithin a team of therapeutic and regulatory experts - Defined CRApromotion and growth ladder with potential for mentoring andmanagement advancements - Competitive pay and opportunity forsignificant travel bonus Responsibilities - Conduct qualification,initiation, monitoring, and closeout visits for research sites incompliance with the approved protocol; - Communication with themedical site staff including coordinators, clinical researchphysicians and their site staff; - Verifying adequate investigatorqualifications, training and resources, including facilities,laboratories, equipment, and staff; - Medical record and researchsource documentation verification against case report form data,including informing the site staff of any entry errors, ensuringgood documentation practices are being adhered to and communicatingprotocol deviations appropriately per SOPs, GCP and applicableregulatory requirements; - Verification that the investigator isenrolling only eligible subjects; - Regulatory document review; -Medical device and/or investigational product/drug accountabilityand inventory; - Verification and review of adverse events, seriousadverse events, concomitant medications and corresponding illnessesto confirm accurate data reporting in accordance with the protocol;- Assessing the clinical research site’s patient recruitment andretention success and offering suggestions for improvement; -Completion of monitoring reports and follow-up letters, whichincludes providing summaries of the significant findings,deviations, deficiencies, and recommended actions to securecompliance. Qualifications - Minimum of a bachelor’s degree; Healthor life science related field preferred; - Willing to travelapproximately 60-80% nationally; - Familiarity with Microsoft®Office; and - Strong communication and presentation skills a plus.- Must hold a valid drivers licence Medpace Overview Medpace is afull-service clinical contract research organization (CRO). Weprovide Phase I-IV clinical development services to thebiotechnology, pharmaceutical and medical device industries. Ourmission is to accelerate the global development of safe andeffective medical therapeutics through its scientific anddisciplined approach. We leverage local regulatory and therapeuticexpertise 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 UsToday. The work we’ve done over the past 30+ years has positivelyimpacted the lives of countless patients and families who facehundreds of diseases across all key therapeutic areas. The work wedo today will improve the lives of people living with illness anddisease in the future. Medpace Perks - Flexible work environment -Competitive compensation and benefits package - Competitive PTOpackages - Structured career paths with opportunities forprofessional growth - Company-sponsored employee appreciationevents - Employee health and wellness initiatives Awards -Recognized by Forbes as one of America's Most Successful MidsizeCompanies in 2021, 2022, 2023 and 2024 - Continually recognizedwith CRO Leadership Awards from Life Science Leader magazine basedon expertise, quality, capabilities, reliability, and compatibilityWhat to Expect Next A Medpace team member will review yourqualifications and, if interested, you will be contacted withdetails for next steps. EO/AA EmployerM/F/Disability/Vets
