iqvia

¡Únete a nosotros y descubre un lugar donde puedes crecer y desarrollarte profesionalmente, innovar y transformar la vida de los pacientes! Te ofrecemos un entorno laboral global que es inclusivo, respetuoso e innovador. Somos una empresa que valora la igualdad de oportunidades y se enorgullece de s

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, besse

Shape the Future of a Rapidly Growing Business IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analyt

Visão geral do trabalho Maximizar o crescimento das vendas em um território geográfico específico, de acordo com a estratégia e os objetivos da empresa. Funções essenciais •Realizar visitas a médicos e outros profissionais importantes na estrutura decisória de hospitais e outras instituições de saúd

Missão do Cargo:Atuar na navegação e acompanhamento do paciente ao longo de toda a jornada de cuidado, promovendo acesso adequado aos serviços de saúde, orientação qualificada e articulação com os diferentes stakeholders do ecossistema, com foco em experiências complexas, como doenças raras e oncolo

Office Locations: Boston, MA San Francisco, CA The IQVIA Market Access Strategy Consulting team (formerly known as Amundsen Consulting), is a market-leading strategy and analytics division within IQVIA that helps manufacturers in the pharmaceutical and biotechnology industry meet the challenges of t

Overview Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations, guide

Job Description Summary Responsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representativ

Job OverviewUnder general supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also in

Je bezoekt apotheken binnen jouw regio en biedt ondersteuning en service aan. Daarnaast ben je verantwoordelijk voor order taking. Jij maakt het verschil, want 🃏 je bent positief, creatief en innovatief, 🃏 je bent het luisterend oor dat de noden van de klant ontdekt 🃏 je bent gepassioneerd en ondern

Local de atuação: Brasília/DF Principais Responsabilidades Promover e gerar demanda dos produtos da linha de Oftalmologia junto a médicos e demais profissionais de saúde. Desenvolver relacionamento estratégico com oftalmologistas, clínicas e hospitais da região. Executar o plano de visitação médica,

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, init

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU)

Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.• Assist the clinical tea

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we support innovation from concept to commercialization, offering expertise in regulatory strategy, clinical

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we support innovation from concept to commercialization, offering expertise in regulatory strategy, clinical

Job OverviewUnder general supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also in

We are seeking an Associate Scientist, Lab Operations to join IQVIA Laboratories at Valencia, CA. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate r

We are seeking a Histologist 1 to join IQVIA Laboratories at Valencia, CA. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development

Due to sponsor requirements, only candidates with a strong Oncology background will be considered for the role Why Join Global Study Leadership? Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and customer-dedicated delivery mode