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Browse fresh roles from company career pages, then filter by keyword, location, salary, skills, remote scope, and more. Each listing links back to the employer-controlled apply path when available.
Browse fresh roles from company career pages, then filter by keyword, location, salary, skills, remote scope, and more. Each listing links back to the employer-controlled apply path when available.
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Location On-site role in Irving, TX. Job Summary The Administrative Assistant will provide administrative support. Essential Duties and Responsibilities Essential and other important responsibilities and duties may include but are not limited to the following: Schedule inter
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Roles and Responsibilities Ensures that the appropriate processes are adequately documented and followed across all systems. Converts data received from the data suppliers into IQVIA standard format as per instructions. Received sales, product, manufacturer, and customer files
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Atividades: Suporte na gestão de projetos de pesquisa de mercado Desenvolver questionários de pesquisa de mercado Analisar as respostas dos médicos às questões de pesquisa de mercado Elaboração de gráficos que mostrem claramente os resultados Montagem de apresentações finais
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Project Management Analysts (PMA) 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 PMA works in partnership with the Project Leader (PL)/Clinical Project Manager (CPM) providin
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We are seeking an experienced Statistical Programming Manage to support the delivery of statistical programming activities for studies involving Swedish health data in our RWE BIOS team . This role requires strong technical expertise, hands-on programming experience, and the abi
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Atividades: Suporte na gestão de projetos de pesquisa de mercado Desenvolver questionários de pesquisa de mercado Analisar as respostas dos médicos às questões de pesquisa de mercado Elaboração de gráficos que mostrem claramente os resultados Montagem de apresentações finais
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Visão Geral: Buscamos um(a) profissional residente no Rio de Janeiro/RJ para atuar como Gerente Distrital de Força de Vendas, com forte capacidade de liderança, excelente comunicação e foco em resultados. Essa posição é responsável por gerir equipes de campo, impulsionando a per
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The IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client’s project team to set-up and execute clinical trials. As Clinical Trial Leader (m/w/d) you will be accountable for the operational performance of
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Job Overview We are seeking a skilled and motivated Senior .NET Software Engineer with a strong background in building scalable, high-performance applications. The ideal candidate will have hands-on experience across the Microsoft technology stack, including .NET Core, ASP.NET M
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Job Overview: Associate Clinical Lead Directors are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Clinical Lead Director is a member of the core projec
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JOB DESCRIPTION: • Under close guidance or supervision, responsible for creating and maintaining the IQVIA reference database ROLES and ACCOUNTABILITIES: • Perform research (internet search; source books, etc.) to gather information from third parties that will augment the com
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Our MedTech Healthcare Collection Associate will be responsible for collecting reprocessed medical equipment in a hospital. You will be working with surgical, non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing Departmen
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This is an exciting opportunity to join IQVIA as an Oncology Hybrid Sales Specialists working closely with Johnson and Johnson client partners resource teams to advance the proper care and use of the available Lung Oncology Portfolio. Territory size and scope of coverage can vary
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Job Overview A Central Monitor is a key skilled and clinically experienced team member of IQVIA Central Monitoring Department. Provides remote project support and assistance across multiple projects, sites and teams and reviews the structured clinical data output with access to
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Role Purpose: Under close guidance or supervision, responsible for creating and maintaining the IQVIA outlet database. Job Description: Perform daily maintenance of outlet master file for US production. Solicits, gathers, and validates information from different sources to id
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Valorizamos a diversidade e acreditamos em equipes inclusivas. Por isso, esta é uma vaga afirmativa destinada a pessoas com deficiência (PCDs). Responsabilidades: Aprovação do registro contábil e pagamentos de notas fiscais de fornecedores, taxas e impostos. Realizar lançament
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We are seeking experienced laboratory professionals to join the Project Services team at IQVIA Laboratories. This role is 100% remote (Pacific Time business hours). We are hiring at multiple levels — candidates are aligned to the appropriate level based on experience. We hire p
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Job Level: Remote Visit Coordinator, US Regional Specialist Location: Home-based in USA Job Overview Regional Specialists (RS) are an integral part of Remote Research Clinicians (RRC) visit delivery, serving as a key liaison between clinical teams, remote research clinicians,
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We are seeking experienced laboratory professionals to join the Project Services team at IQVIA Laboratories. This role is 100% remote (Eastern Time business hours). We are hiring at multiple levels — candidates are aligned to the appropriate level based on experience. We hire p
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Job Overview As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities. Review, assess, and process safety data and information received from various sources. Distribute reports/data to internal and external third parties
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We are seeking a highly motivated pharmacovigilance professional to join our Safety Aggregate Report & Analytics (SARA) team. This is an exciting opportunity to take a leading role in safety reporting, signal management, and benefit-risk evaluation activities supporting both mark
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Job Overview: The Medical Information Case Processor responsibilities include receiving and documenting incoming telephone calls or emails from investigative sites or other sources reporting Lifecycle Safety Data. Responsibilities include: Medical Information Case processor re
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Job Overview As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities. Review, assess, and process safety data and information received from various sources. Distribute reports/data to internal and external third parties
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As Strategic Partnerships Manager (Healthcare Data), you will lead the strategy, development, and management of IQVIA's data supplier ecosystem in Belgium and Luxembourg. You will drive strategic partnerships, data acquisition performance, and operational excellence to ensure sus
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Shape the Future of Responsible Healthcare Data At IQVIA, we help healthcare organizations accelerate innovation and improve patient outcomes through the power of data, technology, and human science. We are looking for an Information Governance & Privacy Manager to lead and str