📑 **Overview** Individuals joining us are assured of a rewarding and progressive career in life sciences consulting. You’ll have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in delivering solutions. We operate in a truly multi-cultural, collegial and collaborative work ...
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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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📑 **Job Overview** Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. **Fluent in Dutch and English.** **Essential Functions** < ...
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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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📑 Overview Individuals joining us are assured of a rewarding and progressive career in life sciences consulting. You’ll have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in delivering solutions. We operate in a truly multi-cultural, collegial and collaborative work en ...
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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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📑 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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📑 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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📑 Job Overview Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. Fluent in Dutch and English. Essential Functions <l ...
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📑 Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and medical 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 accelerate innovation for a h ...
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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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📑 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 analy ...
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📑 As our next Finance Analyst at IQVIA NL, you will be responsible for managing the IQVIA NL **Finance Planning & Analysis function across all BUs of our Dutch entity** . _IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed thro ...
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📑 **Job Family:** Consulting Services **Location:** [EU-Wide] **Real World Commercial Solutions to Create a Healthier World** In RWCS we’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops ...
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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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📑 **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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📑 We are looking for a Principal Life Sciences to join the Dutch Analytics Solutions & Consulting team at IQVIA Netherlands, reporting into the Director Analytics Solutions & Consulting. In this role, you will be involved in client/project leadership, business development, and people/operational leadership to support clients that are based in the Net ...
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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, I ...
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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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📑 **Real World Commercial Solutions to Create a Healthier World** In RWCS we’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence-based strategies that are used in published research, clinical guidelines, and market acce ...
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📑 **Principal / Senior Principal - Value and Payer Evidence, Strategy Consulting, EMEA** **Overview** IQVIA™ (www.IQVIA.com) is the world’s leading company providing information, technology, and services for virtually every type of stakeholder in healthcare to accelerate innovation for a healt ...
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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 Nijmegen. This freelance role is for **20 hours** per week and is expected to last approximately 12-17 months. The successful candidate will be responsible for suppo ...
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📑 Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Site Research Assistant to support a site in Rotterdam. This part-time, freelance role is for **20 hours** per week and is expected to last approximately 12-17 months. The successful candidate will be responsible for ...
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📑 **Job Overview** The Vice President Medical Strategy and Head of the Hematology/Oncology COE provides strategic medical and scientific leadership, subject matter experience and expertise to IQVIA and to IQVIA’s clients in Hematology and Oncology. The overarching remit is to grow IQVIA’s market share in hematology and oncology and ...
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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 Groningen. This freelance role is for **21 hours** per week and is expected to last approximately 12-17 months. The successful candidate will be responsible for supp ...
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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 one or several sites in Amsterdam. This freelance role is for **16-40 hours** per week and is expected to last approximately 12-17 months. The successful candidate will be res ...
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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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📑 **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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📑 **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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📑 **Senior Consultant, Statistics & Psychometrics** **Location** : Greece, Germany, UK, Spain, Netherlands, Portugal, Bulgaria, Slovakia & Estonia. **Work Model** : Hybrid or Office based **The Role:** The Psychometrician will be esponsible for the on-time completion of projects or components of ...
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📑 **Location:** EU Wide or London/Cambridge/Paris/Munich/Madrid/Basel an Amsterdam. **Real World Commercial Solutions to Create a Healthier World** In RWCS we’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develo ...
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📑 Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and medical 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 accelerate innovation for ...
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📑 Regulatory Affairs, Associate Apply now » Date:Apr 25, 2024 Location: Hilversum, North Holland, NL, 1221JT Company: IFF Family of Companies Job Description The regional Reg ...
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📑 You will lead the Regulatory Affairs team for Digital and Computational Pathology (DCP) solutions, a part of the Diagnostic and Pathway Informatics (DPI) business within Precision Diagnosis. The DCP solutions allow (amongst others) fast first-time-right scanning and support multi-disciplinary patient data review and care pathway selection. Leading ...
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📑 My client, a forward-thinking medical device company at the forefront of bioelectronic medicine. Their mission is simple, they're set to revolutionise healthcare by developing cutting-edge therapies for individuals battling chronic diseases. With their breakthrough, they have been granted the Breakthrough Device Designation by the United States ...
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📑 As our next Finance Analyst at IQVIA NL, you will be responsible for managing the IQVIA NL Finance Planning & Analysis function across all BUs of our Dutch entity . IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through ...
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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, techno ...
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📑 Job description About Us: We are a leading company dedicated to healthcare, engineering, and pharmaceutical innovations. As we continue to expand our impact on global health, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. Our organization is comm ...
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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, techno ...
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📑 Senior QA Associate - 2406183529W **Description** We are seeking a highly skilled and motivated Risk Management and Regulatory Compliance Specialist to join our team. In this role, you will be responsible for leading various aspects of risk management, regulatory compliance, and governance activities within our QA Organiz ...
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📑 Job Summary Support QA&RA manager in driving Quality & Regulatory compliance while aligning with the overall organization to meet business needs & objectives Support maintenance of Technical dossiers – including preparing necessary documentation - for all Quirem Medical’s products. Technical dossiers suppor ...
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📑 **For Current Kite Pharma Employees and Contractors:** Please log onto your Internal Career Site (~/cacheable-task/2997$2151.htmld#backheader=true) to apply for this job. At Kite, we empower our leaders to step up, share ideas, listen ...
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📑 **Job Overview:** As Senior Authority/Regulatory Compliance Engineer you will be accountable for ensuring compliance to country specific regulatory requirements and development of certification schemes for our Energy Transition projects in Europe. You will bring your experience in certification compliance schemes and understandin ...
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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 advanced a ...
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📑 About the Role We are looking for an experienced assistant general counsel to help ensure the company complies with the evolving crypto regulatory framework in the UK and EMEA, as well as assist with core regulatory compliance issues for our global entities including with regards to data privacy. Day to day duties will range from regulato ...
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📑 NTT is a leading global IT solutions and services organisation that brings together people, data and things to create a better and more sustainable future. In today’s ‘iNTTerconnected’ world, connections matter more now than ever. By bringing together talented people, world-class technology partners and emerging innovators, we h ...
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📑 **Job Description** At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career g ...
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📑 Senior Legal Counsel - Regulatory Law EMEA - 2406180718W **Description** At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Thr ...
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📑 Senior Legal Counsel - Regulatory Law EMEA - 2406180718W **Description** At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Thr ...
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