Experienced Clinical Research Associate, Iqvia Biotech
2 settimane fa
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.• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.QualificationsUniversity Bachelor's Degree and Master's Degree in scientific discipline or health careIn possession of CRA Certification as required by Ministerial Decree datedExperience in Pharma Industry, and/or Clinical Trials environmentVery good computer skills including MS OfficeExcellent command of English languageOrganizational, time management and problem-solving skillsAbility to establish and maintain effective working relationships with coworkers, managers, and clientsFlexibility to travelDriver's license class BIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide .Learn more at
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milano, Italia IQVIA LLC A tempo pienoExperienced 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: R Job Overview:Perform monitoring and site management work to ensure that sites are conducting the...
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Experienced Clinical Research Associate, IQVIA Biotech
4 settimane fa
Milano, Italia IQVIA A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, Italy 2 days ago Be among the first 25 applicants 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....
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Experienced Clinical Research Associate, IQVIA Biotech
2 settimane fa
milano, Italia IQVIA A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, Italy1 day ago Be among the first 25 applicantsJob OverviewPerform 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...
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Via Milano, Italia IQVIA A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, Italy1 day ago Be among the first 25 applicantsJob OverviewPerform 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...
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Experienced Clinical Research Associate, IQVIA Biotech
2 settimane fa
Via Milano, Italia IQVIA A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, Italy 1 day ago Be among the first 25 applicants 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...
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Milano, Italia Wolters Kluwer A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, ItalyTheForkRemotoEUR ***************3 giorni faPerform 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...
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Milano, Italia Wolters Kluwer A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, ItalyTheForkRemotoEUR ***************3 giorni faPerform 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...
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Experienced Clinical Research Associate, Iqvia Biotech
2 settimane fa
Milano, Italia Altro A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, Italy1 day ago Be among the first 25 applicantsJob OverviewPerform 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...
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milano, Italia TheFork A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, ItalyRemotoEUR 40.000 - 60.000Milan, ItalyPerform 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 FunctionsPerform...
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Milano, Italia Thefork A tempo pienoExperienced Clinical Research Associate, IQVIA Biotech - Home based, ItalyRemotoEUR ***************Milan, ItalyPerform 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 FunctionsPerform...
