Lavori attuali relativi a Experienced Clinical Research Associate - WorkFromHome - Medpace
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Clinical Research Associate
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WorkFromHome, Italia PHIDEALIVE Srl A tempo pienoCompany Description Phidealive, established in 2018, is a Contract Research Organization (CRO) with a strong foundation in Italy’s rich clinical research culture. Positioned as a Clinical Research Atelier, Phidealive emphasizes scientific rigor, regulatory compliance, and a tailored operational approach for each project. The company collaborates with...
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WorkFromHome, Italia Medpace A tempo pienoOur clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous...
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WorkFromHome, Italia TFS HealthScience A tempo pienoA leading global Contract Research Organization is seeking a Clinical Research Associate to remotely monitor clinical trials in Italy. The ideal candidate will have a bachelor's degree, over 2 years of CRA experience in oncology, and strong communication skills. Responsibilities include ensuring compliance with clinical procedures and regulatory...
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WorkFromHome, Italia ICON A tempo pienoA leading healthcare company is looking for a Clinical Research Associate II to join their dynamic team in Milan. The role involves conducting clinical trial visits, ensuring protocol compliance, and maintaining data integrity. Candidates should have a Bachelor's degree in a relevant field and experience as a Clinical Research Associate. This position...
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Clinical Research Associate
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WorkFromHome, Italia TFS HealthScience A tempo pienoOverview CLINICAL RESEARCH ASSOCIATE - REMOTE BASED (ITALY) TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and functional service (FSP)...
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WorkFromHome, Italia Medpace A tempo pienoA clinical contract research organization is seeking a full-time Clinical Research Associate to join their Clinical Monitoring team in Italy. The role involves conducting site visits, ensuring compliance with protocols, and requires a Master's degree in a health-related field along with CRA certification. Candidates must be fluent in English and Italian and...
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Clinical Research Associate I — Global Travel
52 minuti fa
WorkFromHome, Italia ICON A tempo pienoUn'importante organizzazione di ricerca clinica è alla ricerca di un Clinical Research Associate I. Il candidato ideale ha una laurea in campo scientifico e almeno un anno di esperienza nel monitoraggio clinico. È in grado di lavorare in team e ha attenzione ai dettagli. La posizione richiede viaggi frequenti e rappresenta un'opportunità di crescita in un...
Experienced Clinical Research Associate
6 ore fa
Our clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Medpace will provide comprehensive initial and ongoing training depending on your previous experience. Responsibilities Conduct 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. Qualifications Master degree in health-related field; CRA certification completed as per DMC 15 /11 / 2011; Previous experience as CRA; Willing to travel up to 60-80% nationally; Familiarity with Microsoft® Office; Fluent in English and Italian language; Strong communication and presentation skills would be considered as a plus. Medpace Overview Medpace 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 Perks Flexible 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 initiatives Awards Recognized 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 compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. #J-18808-Ljbffr
