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📑 **With approximately 70,000 employees in more than 100 countries, IQVIA is in a truly unique position to be able to support companies seeking to improve real-world patient outcomes and enhanced clinical trial outsourcing through treatment innovations, care provision and access. With a broad range of healthcare information, technology and service of ...

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📑 **Join us on our exciting journey!** We are looking for a **Team Leader Regulatory Editor** , this could be your chance to start a new adventure in a company with the best Regulatory Talents. In this role you will be joining part of a new team of experienced regulatory intelligence analysts during a period of strong growth. Working in a ...

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📑 Clinical Project Management services provides local management of a clinical trial (or Medical Affairs data generation activity) across Belgium. Services/deliverables include operational oversight of assigned protocols at the country level from start-up through to database lock and closeout activities. Further, services will ensure the local trial ...

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📑 **Job Overview:** Local Clinical Project Management services provides local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned protocol(s) at the country level from start-up through to database lock and closeout activities. Fu ...

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📑 **PURPOSE** You will be a member of the new IQVIA financial shared services center in Bratislava Slovakia, supporting our operations in EMEA, which is an integral part of our global financial shared services network. On this position, you will assist the Team Leader responsible for the accounting and reporting requirements for the Com ...

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📑 Join our rapidly growing sponsor-dedicated team as a **Local Trial Manager** ! Home-based working with minimal travel, open to candidates across Denmark. As Local Trial Manager you will be responsible for running international/global studies in all therapeutic areas, managing the operational aspects of projects to meet contractual re ...

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📑 **Join us in our exciting journey!!** **IQVIA is expanding in EMEA!!** We currently have a Regional CPM **to work sponsor-dedicated** to one of our pharmaceutical clients The Clinical Trial Manager (CTM) is accountable for the operational and scientific oversight, the set-up, execution and delivery of their assigned clinical trials ...

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📑 **Join us on our exciting journey!** 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, t ...

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📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

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📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

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📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

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📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

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📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

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📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

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📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

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📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

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📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

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📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job

📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job

📑 **Flexible location across Europe** **Job Overview** You will be responsible for overseeing complex project delivery lead by the EMEA PPG Software Development & Support Team to our EMEA Provider, Payer and Government clients, as well as ensuring post go-live/BAU support is in place. Your will be responsible for the regional PPG Delive ...

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📑 With approximately 85,000 employees in more than 100 countries, IQVIA is in a truly unique position to be able to support companies seeking to improve real-world patient outcomes and enhanced clinical trial outsourcing through treatment innovations, care provision and access. With a broad range of healthcare information, technology and service offe ...

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📑 IQVIA currently offers the exciting opportunity for a **Junior Study Start-Up / Site Activation Specialist (m/w/d)** to work in the Country Site Activation Department in our **Frankfurt or Vienna office** or in **home office throughout Germany or Austria** . In this role you will perform tasks at a country level (Germany and/or Austria) ...

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📑 **Job 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' experience with ...

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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' experience with ...

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📑 **Job 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. **Fluent in both Swedish and English.** ...

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📑 **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 and guidelines, and sponsor requirements. **Essential Functions** • Perform site monitoring visits (selection, initiation, monitoring and clos ...

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📑 **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 and guidelines, and sponsor requirements. **Essential Functions** • Perform site monitoring visits (selection, initiation, monitoring and clos ...

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📑 **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 and guidelines, and sponsor requirements. **Essential Functions** • Perform site monitoring visits (selection, initiation, monitoring and clos ...

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📑 **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 and guidelines, and sponsor requirements. **Essential Functions** • Perform site monitoring visits (selection, initiation, monitoring and clos ...

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📑 IQVIA is hiring a Clinical Trials Coordinator (trilingual) to provide service to one of our sponsors a well known pharma company with offices in Brussels to support the submissions, budgeting, agreement and payments. **Your duties** + Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) + Ensure collation and dis ...

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📑 **Job Overview** Data access expertise to complete and manage the data permit processes, data extraction processes and data providers engagements. Holistic knowledge about local data providers and data availability in national and quality registries. Data access expertise to complete feasibility study tasks across all workstreams, to manage ...

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📑 **PURPOSE** **Engage in company training program to gain knowledge and skills required to provide administrative support to projects in accordance with SOPs, policies, good clinical practices, and applicable regulatory requirements. Meeting quality and timeline metrics under direction of line manager and/or other designated team members.** ...

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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, technology, anal ...

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