Lavori attuali relativi a Clinical Research Associate - Turin - Altro
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Clinical Research Associate
4 settimane fa
Turin, 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
3 giorni fa
Turin, Italia AL Solutions A tempo pienoClinical Research Associate – International CRO – ItalyMy client, an international mid-sized CRO, is seeking an experienced CRA to support and take responsibility for a Phase 3 study in France. We're looking for someone who works confidently on their own, shows strong proactivity, and is highly quality focused.Key Responsibilities:Oversight and...
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Clinical Research Associate
1 giorno fa
Turin, Italia AL Solutions A tempo pienoClinical Research Associate – International CRO – ItalyMy client, an international mid-sized CRO, is seeking an experienced CRA to support and take responsibility for a Phase 3 study in France. We’re looking for someone who works confidently on their own, shows strong proactivity, and is highly quality focused.Key Responsibilities:Oversight and...
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Clinical Research Associate
3 giorni fa
Turin, Italia AL Solutions A tempo pienoClinical Research Associate – International CRO – Italy My client, an international mid-sized CRO, is seeking an experienced CRA to support and take responsibility for a Phase 3 study in France. We’re looking for someone who works confidently on their own, shows strong proactivity, and is highly quality focused. Key Responsibilities: - Oversight and...
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Clinical Research Associate
3 giorni fa
Turin, Italia AL Solutions A tempo pienoClinical Research Associate – International CRO – Italy My client, an international mid-sized CRO, is seeking an experienced CRA to support and take responsibility for a Phase 3 study in France . We're looking for someone who works confidently on their own, shows strong proactivity, and is highly quality focused. Key Responsibilities: Oversight and...
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Clinical Research Associate
2 giorni fa
Turin, Italia AL Solutions A tempo pienoClinical Research Associate – International CRO – ItalyMy client, an international mid-sized CRO, is seeking an experienced CRA to support and take responsibility for a Phase 3 study in France. We’re looking for someone who works confidently on their own, shows strong proactivity, and is highly quality focused.Key Responsibilities:- Oversight and...
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Clinical Research Associate
2 giorni fa
Turin, Italia AL Solutions A tempo pienoClinical Research Associate – International CRO – ItalyMy client, an international mid-sized CRO, is seeking an experienced CRA to support and take responsibility for a Phase 3 study in France. We’re looking for someone who works confidently on their own, shows strong proactivity, and is highly quality focused.Key Responsibilities:- Oversight and...
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Clinical Research Associate
1 giorno fa
Metropolitan City of Turin, Italia AL Solutions A tempo pienoClinical Research Associate – International CRO – Italy My client, an international mid-sized CRO, is seeking an experienced CRA to support and take responsibility for a Phase 3 study in France . We’re looking for someone who works confidently on their own, shows strong proactivity, and is highly quality focused. Key Responsibilities: Oversight and...
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Senior Clinical Research Associate
3 settimane fa
Turin, Italia Teleflex A tempo pienoPOSITION SUMMARY: The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO 14155, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified by the...
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Clinical Research Professional
3 settimane fa
Turin, Italia beBeeCompliance A tempo pienoSenior Clinical Research Associate Role Key Responsibilities include conducting monitoring visits and ensuring compliance with regulatory standards. Responsible for scheduling and conducting on-site and remote monitoring visits. Ensure data accuracy and subject safety. Requirements: Scheduling and Conducting Monitoring Visits Data Accuracy and Subject Safety...
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 have 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 offer diverse 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 accordance 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 for 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 understanding of ICH GCP and applicable regulations; excellent communication skills; ability to multitask and work under demanding timelines.#J-18808-Ljbffr
