Clinical Research Associate
2 settimane fa
Social network you want to login/join with:CliniRx has a number of CRA positions available to support a global study in Q1 2025.We are expanding rapidly and offer multiple permanent opportunities to join us on a global study. Ideally, candidates will come from a CRO background with experience across multiple therapeutic areas.As a global contract research organization (CRO), we provide a diverse range of clinical development and resource solutions, reflecting both full-service CRO and functional service provider (FSP) models. We support clinical outsourcing needs for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises facing unique challenges. Our presence includes the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia.------------------------------------------------------------Primary Purpose:We are seeking skilled CRAs to ensure the timely and high-quality delivery of site monitoring activities in line with our Site Monitoring Plan (SMP).Key Responsibilities:Deliver on the Site Monitoring Plan: Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality standards and timelines.Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.Site Identification: Assist in identifying new potential sites across various therapeutic areas to expand our clinical network.Continuous Skill Development: Regularly improve technical and soft skills to enhance performance and project outcomes.Work Relations:Report to the Manager of Clinical Operations regarding project, functional, and administrative matters.Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff.Value Added:Your adherence to quality standards and timelines in monitoring activities is crucial for the successful delivery of our projects.Key Success Factors:Timely and high-quality execution of site monitoring activities.Prompt report generation and submission to stakeholders.Education: Bachelor’s or Master’s degree in a scientific discipline.Experience: 1-4 years in site monitoring within clinical research.Skills: Strong knowledge of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication skills; ability to multitask and perform under demanding deadlines.#J-18808-Ljbffr
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Clinical Research Associate
4 settimane fa
Milano, Italia Medpace A tempo pienoJoin to apply for the Clinical Research Associate role at Medpace Continue with Google Continue with Google Join to apply for the Clinical Research Associate role at Medpace The 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...
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Clinical Research Associate
1 settimana fa
milano, Italia PHIDEALIVE Srl A tempo pienoCompany DescriptionPhidealive, 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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Clinical Research Associate
2 settimane fa
Milano, 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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Clinical Research Associate
2 settimane fa
Milano, 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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Clinical Research Associate
2 settimane fa
Milano, 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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Clinical research associate
2 settimane fa
Milano, 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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Clinical research associate
2 settimane fa
Milano, 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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Clinical Research Associate
2 settimane fa
Milano, Italia ICON A tempo pienoClinical Research Associate, China ICON 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 Clinical Research Associate to join...
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Milano, Italia ICON A tempo pienoA global clinical research organization in Milan is seeking a Clinical Research Associate to manage all phases of clinical trials. This role involves ensuring protocol compliance and data integrity while collaborating with site staff and investigators. The ideal candidate holds a Bachelor's degree in a relevant field, has extensive experience as a Clinical...
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Clinical Research Associate I – Global Monitoring
1 settimana fa
Via Milano, Italia ICON A tempo pienoA global clinical research organization in Milan is seeking a Clinical Research Associate to manage all phases of clinical trials. This role involves ensuring protocol compliance and data integrity while collaborating with site staff and investigators. The ideal candidate holds a Bachelor's degree in a relevant field, has extensive experience as a Clinical...
