Lavori attuali relativi a Experienced clinical research associate, iqvia biotech - Milan - Scienza Ricerca Sviluppo
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Clinical Research Associate
3 settimane fa
Milan, 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
3 settimane fa
Milan, 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
3 settimane fa
Milan, Provincia di 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
3 settimane fa
Milan, 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
3 settimane fa
Milan, 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 Vendor Manager
1 settimana fa
Milan, Italy (ITALY, ) IQVIA A tempo pienoOn behalf of our Client a global pharmaceutical company, IQVIA is looking for Vendor Management Lead, Drug Development.The profile will be responsible for selection, contracting, oversight, and performance management of external vendors and collaborators based in Italy, supporting clinical development. External vendors include CROs, CMOs, central labs and...
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Clinical Research Associate
1 settimana fa
Milan, Italia OPIS A tempo pienoLocalitàProvince of Monza and Brianza, Italy Azienda OPIS - Guarda altre offerteLocalitàProvince of Monza and Brianza, Italy Descrizione Participate in the feasibility process of new studies/clinical investigations, collect feasibility questionnaire (if applicable) and other documents necessary for the ethical and administrative (…)Perform...
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Product Specialist Oncology
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Milan, Italia IQVIA Italia A tempo pienoIn order to create a new project linked to oncology therapy area, IQVIA is looking for Territory Sales Specialist who can join an exciting working environment in a dynamic atmosphere. Role Purpose To maximize sales within a specified geographical territory, consistent with our strategy and objectives. Work as a product sales specialist within the oncology...
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Accountant & Controller-Azienda Farmaceutica
2 giorni fa
Milan, Provincia di Milano, Italia IQVIA Italia A tempo pienoOn behalf of our Client a global pharmaceutical company, IQVIA is looking for an Accountant & Controller who can join an exciting working environment in a dynamic atmosphere. The position will be based in our Milan office. RESPONSIBILITIES: As part of the company's growth and further professionalization, we are now looking for an experienced, proactive and...
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Credit Collector
2 giorni fa
Milan, Provincia di Milano, Italia IQVIA Italia A tempo pienoOn behalf of our Client a global pharmaceutical company, IQVIA is looking for a Field Collector & Credit Management who can join an exciting working environment in a dynamic atmosphere. Position Overview We are seeking a highly motivated Field Collector & Credit Management professional to join our team. The ideal candidate will be responsible for performing...
Experienced clinical research associate, iqvia biotech
2 giorni fa
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy page is loaded## Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italylocations:Milan, Italytime type:Full timeposted on:Posted Todayjob requisition id:R1501739 Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions:• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
