Clinical Research Associate
8 ore fa
Clinical Research Associate - Remote - USICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team.As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.What you will be doingConducting site qualification, initiation, monitoring, and close-out visits for clinical trials.Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.Collaborating with investigators and site staff to facilitate smooth study conduct.Performing data review and resolution of queries to maintain high-quality clinical data.Contributing to the preparation and review of study documentation, including protocols and clinical study reportsYour profileBachelor's degree in a scientific or healthcare-related field.Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.Strong organizational and communication skills, with attention to detail.Ability to work independently and collaboratively in a fast-paced environment.Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's licenseWhat ICON can offer you:Our success depends on the quality of our people.That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.In addition to your competitive salary, ICON offers a range of additional benefits.Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our benefits examples include:Various annual leave entitlementsA range of health insurance offerings to suit you and your family's needs.Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.Life assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.Visit our careers site to read more about the benefits ICON offers.At ICON, inclusion & belonging are fundamental to our culture and values.We're dedicated to providing an inclusive and accessible environment for all candidates.ICON is committed to providing a workplace free of discrimination and harassment.All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request hereInterested in the role, but unsure if you meet all of the requirements?We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.Are you a current ICON Employee?Please click here to apply#J-*****-Ljbffr
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Clinical Research Associate
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Clinical Research Associate
4 settimane fa
Milano, Italia MCR - Mediolanum Cardio Research s.r.l. A tempo pienoMediolanum Cardio Research è alla ricerca di un/a Clinical Research Associate (CRA) certificato/a di talento e motivato/a per unirsi al nostro team di ricerca clinica. Responsabilità Principali Il candidato ideale sarà responsabile della gestione e del monitoraggio delle attività degli studi clinici in conformità con i protocolli di ricerca, le Good...
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Clinical Research Associate
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Milano, Italia Medpace A tempo pienoJoin to apply for theClinical Research Associaterole atMedpaceContinue with Google Continue with GoogleJoin to apply for theClinical Research Associaterole atMedpaceThe 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...
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Milano, Italia MCR - Mediolanum Cardio Research s.r.l. A tempo pienoMediolanum Cardio Research è alla ricerca di un/a Clinical Research Associate (CRA) certificato/a di talento e motivato/a per unirsi al nostro team di ricerca clinica. Responsabilità Principali Il candidato ideale sarà responsabile della gestione e del monitoraggio delle attività degli studi clinici in conformità con i protocolli di ricerca, le...
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Clinical Research Associate
4 settimane fa
Milano, Italia MCR - Mediolanum Cardio Research s.r.l. A tempo pienoMediolanum Cardio Research è alla ricerca di un/a Clinical Research Associate (CRA) certificato/a di talento e motivato/a per unirsi al nostro team di ricerca clinica. Responsabilità Principali Il candidato ideale sarà responsabile della gestione e del monitoraggio delle attività degli studi clinici in conformità con i protocolli di ricerca, le...
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Clinical Research Associate
4 settimane fa
Milano, Italia MCR - Mediolanum Cardio Research s.r.l. A tempo pienoMediolanum Cardio Research è alla ricerca di un/a Clinical Research Associate (CRA) certificato/a di talento e motivato/a per unirsi al nostro team di ricerca clinica. Responsabilità Principali Il candidato ideale sarà responsabile della gestione e del monitoraggio delle attività degli studi clinici in conformità con i protocolli di ricerca, le Good...