📑 **IQVIA™** is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced ...
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📑 **Job Title:** Project Manager- Strategic Meetings and Events, EMEA **Contract:** Fixed Term **Location:** Greece, Portugal, Poland or South Africa IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. ...
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📑 **IQVIA Safety Operations** team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse team based across the world, with ‘safety hubs’ in Ireland, Poland, Austria, Portugal, Slovakia, S ...
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📑 **IQVIA Safety Operations** team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse team based across the world, with ‘safety hubs’ in Ireland, Poland, Austria, Portugal, Slovakia, S ...
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📑 **Associate Site Manager with French** **Real-World Evidence** Hybrid: EMEA **Join us on our exciting journey!** IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers ...
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📑 **Overview** 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, analytics and human ingenuity to drive healthcare forward. <br ...
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📑 Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. **RESPONSIBILITIES** + Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex + Ability to administratively and te ...
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📑 Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs **RESPONSIBILITIES** + Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Ove ...
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📑 IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and a ...
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📑 **Job Overview** **Responsible for the on-time completion of Quantitative Primary Market Research projects** or components of large, complex projects for clients in the life sciences field. **Main Responsibilities** • Participates or leads projects team members in the design, development and ...
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📑 Job Title: Project Manager- Strategic Meetings and Events, EMEA Contract: Fixed Term Location: Greece, Portugal, Poland or South Africa IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With approximatel ...
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📑 **ob Overview** Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. **_At least 1 years' expe ...
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📑 **Location:** Portugal, Poland, Brazil **Work model:** Hybrid (1-2 days per week in the office) This is one of a key cybersecurity role within the global Information Security organization. The individual fulfilling this Information Security Manager role in Vulnerability Management team will partner c ...
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📑 **Site Contract Manager** **IQVIA cFSP** **Spain and France Home Based** **Join us on our exciting journey!** **Remote/Hybrid/Office based working options.** Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward ...
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📑 **Site Manager Study Start-Up** **Real-World Evidence** EMEA based **Join us on our exciting journey!** IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, provide ...
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📑 **Client Service Specialist** Location: Warsaw **About the Team** In our Client Service department you will be part of a team whose task is to contact IQVIA clients in all matters connected to after-sales and service related to products and services under the care of the department. ...
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📑 **IQVIA is hiring Clinical Research Associates!** Join IQVIA today and make an impact on patients’ outcome! **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 ...
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📑 **Who are we?** We are the creators of ClinSpark®, the world’s first CDISC ODM certified Phase I eSource and clinical trial automation system. ClinSpark (now known as ’IQVIA Clinical eSource) improves the speed, quality and transparency of clinical research. We support a large and growing set of device integrations, enabling data ...
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📑 IQVIA Safety Operations team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse team based across the world, with ‘safety hubs’ in Ireland, Poland, Austria, Portugal, Slo ...
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📑 IQVIA Safety Operations team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse team based across the world, with ‘safety hubs’ in Ireland, Poland, Austria, Portugal, Slo ...
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📑 Overview 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, analytics and human ingenuity to drive healthcare forward. Th ...
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📑 The Sr Cybersecurity Engineer role is a vital part of our Cybersecurity Engineering team in the CISO organization. This is a hands-on security engineering role ensuring the secure operation of the IQVIA global information technology (IT) infrastructure and processes through operating and maintaining our security safeguards. You w ...
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📑 **Who are we?** We are the creators of ClinSpark®, the world’s first CDISC ODM certified Phase I eSource and clinical trial automation system. ClinSpark (now known as ‘IQVIA Clinical eSource Platform’) improves the speed, quality, and transparency of clinical research. We support a large and growing set of device integrations, en ...
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📑 **The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territories and to register several of development projects into the international region. This role is key to driving both the Regulatory strategy and execution.** **• Prov ...
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📑 **Job Overview** As the Senior Solution Specialist in Service Management, you are the subject matter expert in the domain of service management. You will support the design, implementation, and maintenance of customer support models for IQVIA’s clinical eSource platform and digital health/connected device service lines. You are a ...
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📑 Our team is growing, join us on our mission to drive healthcare forward! What We Offer / USPs + The chance to work on cutting edge medicines at the forefront of new medicines development + IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive perfor ...
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📑 Are you interested in collaborating with leading pharma companies to help patients all around the world? When you join IQVIA as a sponsor-dedicated Senior CRA in Poland, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you ...
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📑 Associate Site Manager with French Real-World Evidence Hybrid: EMEA Join us on our exciting journey! IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and patients. ...
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📑 **IQVIA** is the leading **human data science** company focused on helping healthcare clients find unparalleled insights and better solutions for patients. IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. <b ...
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📑 **Join us on our exciting journey!** IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, tech ...
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📑 **Role Overview:** _The Site Enablement Solutions team at IQVIA provides qualified, clinically experienced research staff to clinical trial sites globally to accelerate and optimize the performance of clinical trials. By supplying sites with support for data entry, patient recruitment, patient visits, assessments, and other tasks ...
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📑 **Join us on our exciting journey!** IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, tech ...
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📑 Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Warsaw. This part-time role is for **20 hours** per week and is expected to last approximately 12-17 months. The successful candidate will be responsible for support ...
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📑 Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Bydgoszcz. This part-time role is for **20 hours** per week and is expected to last approximately 12-17 months. The successful candidate will be responsible for supp ...
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📑 About the Role The role of the Client Service Specialist: - very good and the best in class quality of after-sales service towards clients - preparation and delivery of ordered products and services - long-term business relationships and effective cooperation with clients Key Res ...
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📑 **Practice Segment Strategy Lead, Life Sciences** **Team Overview:** IQVIA’s Integrated Health Platform (IHP) is a modern data backbone that enables evolving integration of patient-generated data over time. It supports patient, product, and natural history registries, as well as long-term follow-up (LTFU) in life science studie ...
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📑 **Practice Segment Strategy Lead, Medical Specialties & Healthcare** **Team Overview:** IQVIA’s Integrated Health Platform (IHP) is a modern data backbone that enables evolving integration of patient-generated data over time. It supports patient, product, and natural history registries, as well as long-term follow-up (LTFU) in l ...
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📑 **Job Overview** Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. Developing professional individual contributor who works under moderate supervision. Problems face ...
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📑 **Job Overview** Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. **Essential Functions** • Develop Coordinate the development of investigator gra ...
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📑 Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scie ...
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📑 **Location: Poland or Portugal** **Role:** As a **Senior Information Security Metrics Analyst,** you will play a crucial role in ensuring the security and compliance of our organization. You’ll be responsible for analyzing, measuring, and reporting on various security metrics to enhance our overall security p ...
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📑 **Job Responsibilities** Provide line and functional management of Data Management technical experts, with a team size of around 15-20 people. Manage and prioritize resource assignments, as well as workload management across Technical Design and SAS Programming teams ensuring project milestones are met accordin ...
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📑 Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a ...
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📑 We are currently looking for experienced Front End Developer to join our team. If you are a driven professional with proven experience in the field of frontend development including implementation of UI for web applications, creating documentation and testing. This role could be a stepping stone in your career! **Require ...
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📑 **Role Location: Poland or Portugal** **Job Overview** The successful candidate will play an integral role in developing the information security Risk Management framework for IQVIA and will manage risks identified through a variety of IT and operational audits. You will be responsible for managing the developm ...
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📑 IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based):<br ...
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📑 **Global Data Analyst** **Warsaw, Poland** **(Hybrid)** Research and Insights CoE provides the support in the quantitative market research studies with HCPs and patients/customers at every stage of the project - from pricing to final delivery. The team is based in Poland but as part of a wide ...
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📑 We have great opportunities for those with a background working in Clinical Trials, preferably with a focus on patient recruitment/engagement, to join our Site and Patient Networks team. **PURPOSE** Assist Patient Recruitment Leads and manage assigned tasks related to the coordination, planning, and implementat ...
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📑 **Job Overview** Manages a single department or work unit responsible for site activation. Sets goals and objectives for team members for achievement of short-term operational or tactical results. **_Must have former people management experience._** **Essential Functions** Manages staff's delivery of ...
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📑 Przedstawiciel MedycznyMiejsce pracy: OlsztynTwój zakres obowiązkówPromowanie produktów firmy w środowisku lekarzy i/lub farmaceutów, zgodnie z założoną strategią i prawem farmaceutycznymOdpowiedzialność za realizacje celów sprzedażowychRaportowanie odbytych wizyt w systemie CRM< ...
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