Experienced Cra, Sponsor Dedicated
23 ore fa
Job 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 Functions:• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.• 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.Qualifications:• Bachelor's and Master's Degree in scientific discipline or health care• Requires at least 3 years of year of on-site monitoring experience• In possession of CRA Certification according to Ministerial Decree dated **********• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.IQVIA 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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Experienced Cra, Sponsor Dedicated
23 ore fa
Milano, Italia Iqvia A tempo pienoJob 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...
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Sponsor dedicated CRA I/II
6 ore fa
Milano, Lombardia, Italia サイネオス・ヘルス A tempo pienoUpdated: TodayLocation: Milano, MI, ItalyJob ID: Not ready to apply?Join our Talent NetworkDescriptionSponsor dedicated CRA I/II - Home Based ITASyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to...
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Sponsor dedicated CRA I/II
5 ore fa
Milano, Lombardia, Italia サイネオス・ヘルス A tempo pienoUpdated: December 24, 2025Location: Milano, MI, ItalyJob ID: Not ready to apply?Join our Talent NetworkDescriptionSponsor dedicated CRA I/II - Home based ITASyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into...
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Sponsor dedicated CRA I/II
6 ore fa
Milano, Lombardia, Italia Syneos Health A tempo pienoDescriptionSponsor dedicated CRA I/II - Home based ITASyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the...
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Sponsor Dedicated Cra I/ii
2 settimane fa
Milano, Italia Syneos - Clinical and Corporate - Prod A tempo pieno**Description** Sponsor dedicated CRA I/II - Home Based ITA Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer...
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Sponsor Dedicated Cra Ii/ Sr Cra I
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Milano, Italia Syneos - Clinical and Corporate - Prod A tempo pieno**Description** Sponsor dedicated CRA II/ Sr CRA I - Oncology, Home based ITA Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model...
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Sponsor Dedicated Cra I/Ii
23 ore fa
Milano, Italia Buscojobs IT C2 A tempo pienoSponsor dedicated CRA I/II - Home based ITASyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the...
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Milano, Italia Iqvia A tempo pienoClinical Research Associate, Sponsor Dedicated – ItalyJoin to apply for theClinical Research Associate, Sponsor Dedicated – Italyrole atIQVIAResponsibilitiesPerforming site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with...
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Milano, Italia Iqvia A tempo pienoClinical Research Associate, Sponsor Dedicated – ItalyJoin to apply for theClinical Research Associate, Sponsor Dedicated – Italyrole atIQVIAResponsibilitiesPerforming site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with...
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Sponsor-Dedicated Cra
23 ore fa
Milano, Italia Iqvia A tempo pienoA global leader in clinical research services is seeking a Clinical Research Associate in Milan, Italy.The role involves performing site monitoring, supporting subject recruitment, and ensuring compliance with regulatory standards.Candidates should have a Bachelor's and Master's degree in a relevant field, CRA certification, and experience in the Pharma...
