Experienced Clinical Research Associate, IQVIA Biotech
2 settimane fa
Experienced Clinical Research Associate, IQVIA Biotech - Home based, ItalyOverviewPerform 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. ResponsibilitiesPerform 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 care In possession of CRA Certification as required by Ministerial Decree dated Experience in Pharma Industry, and/or Clinical Trials environment Very good computer skills including MS Office Excellent command of English language Organizational, time management and problem-solving skills Ability to establish and maintain effective working relationships with coworkers, managers, and clients Flexibility to travel Driver's license class B #J-18808-Ljbffr
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Clinical Research Associate
3 settimane fa
Lombardia, 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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Lombardia, Italia IQVIA A tempo pienoOverviewThe Associate Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during the project delivery lifecycle. Provide therapeutic and medical expertise to business development...
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Clinical Research Associate
3 settimane fa
Lombardia, Italia Medpace A tempo pienoClinical Research Associate (CRA) - Law 68/99 Art. 18Join to apply for the Clinical Research Associate (CRA) - Law 68/99 Art. 18 role at Medpace Clinical Research Associate (CRA) - Law 68/99 Art. 18Join to apply for the Clinical Research Associate (CRA) - Law 68/99 Art. 18 role at Medpace Our clinical activities are growing rapidly, and we are currently...
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Sponsor-Dedicated Clinical Project Lead
2 settimane fa
Lombardia, Italia IQVIA A tempo pienoA leading global clinical research provider in Milan is seeking an experienced Clinical Project Manager to oversee the execution of clinical studies. The ideal candidate will ensure project quality and manage cross-functional teams. Strong project management skills are essential, along with a background in life sciences. This role allows for substantial...
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Clinical Project Manager
2 settimane fa
Lombardia, Italia IQVIA A tempo pienoClinical Project Manager - Sponsor Dedicated (9‑month contract)Apply for the Clinical Project Manager - Sponsor Dedicated (9‑month contract) role at IQVIA . Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential...
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Associate Market Access Specialist, South Italy
3 settimane fa
Lombardia, Italia IQVIA A tempo pienoOverviewJoin to apply for the Associate Market Access Specialist, South Italy role at IQVIA . Every 30 minutes, a stroke patient who could have been saved either dies or is permanently disabled because they were treated in the wrong hospital. Our mission is clear: to increase the number of patients treated in stroke-ready hospitals and to optimize the...
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Ass Consultant, Pricing
2 settimane fa
Lombardia, Italia IQVIA A tempo pienoOverviewFor our Real WorldSolution Team in Milan, we are looking for an Analyst/ Ass Consultant to join the Pricing and Market Access. Why to join IQVIAWith IQVIA , you’ll have access to one of the world’s highest-regarded service organizations in the Life Science Sector, providing you with opportunities to work on today’s most challenging,...
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Clinical Research Associate
3 settimane fa
Lombardia, Italia Medpace A tempo pienoJob SummaryOur clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Research Associate (law 68/99 Art. 18) to join our Clinical Monitoring team in Italy. This position will work with a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your...
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Preclinical R&D Director — Biotech Innovation Leader
3 settimane fa
Lombardia, Italia OrgPortunity A tempo pienoA biotech start-up in Lombardia, Monza, is seeking a highly experienced individual to manage preclinical studies and lead R&D teams. The role requires a strong background in Life Sciences, with over 8 years in pharmaceuticals. Responsibilities include planning research initiatives, managing external collaborations, and overseeing regulatory documentation....
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Product Specialist Oncology
4 settimane fa
Lombardia, 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...
