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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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📑 **Clinical Research Associate** IQVIA Belgium is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a me ...

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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** 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. **Required English and Dutch / French language skills.** **Essential Functions** <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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📑 **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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📑 **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 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) ...

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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** **a great team to drive healthcare forward!** The Vaccine solution team consists of enthusiastic consulting professionals with deep expertise & significant experience in the vaccine domain. Our mission is to bring the broad & depth of vaccine knowledge to our corporate consulting organisation in orde ...

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📑 **Job Overview** Clinical Project Management Directors direct and manage the team responsible for clinical delivery of complex; global full service, multi-regional studies and/or programs. Has strategic decision-making responsibility for the project/program. Responsible for direction and management of portfolios and/or accounts f ...

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📑 Clinical Research Associate IQVIA Belgium is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a mean ...

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📑 QVIA is a worldwide top 10 Fortune 500 company, active in Life Sciences. With the merger of Quintiles and IMS Health, IQVIA combines clinical research with a broader use of health data and technology. IQVIA’s data and technology are increasingly used for answering socially relevant questions related to healthcare efficiency, quality and accessibili ...

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📑 Internal Job Description **DevOps Engineer** **Flexible location across Europe, home based** **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 Clinica ...

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📑 Kom werken bij de **IQVIA** familie in het **Omni Care Consult team** . Een toonaangevend bedrijf dat zich specifiek richt op de **zorgsector** . We zijn op zoek naar getalenteerde **Business Analysts** en **Consultants** die samen met ons projecten bij zorgverstrekkers willen realiseren en nauw willen samenwerken met onz ...

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📑 **Clinical Project Manager** The Study Lead Country Operations (SLCO) is the primary point of contact for the Country Operations (CO) team at the global study level and will act as a core study team member. The SLCO will be accountable for coordinating and driving activities performed by country operations including start up, m ...

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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 tr ...

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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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📑 **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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📑 Sales Representatives, Clinical Trial Assistants, Data Consultants, Developers, … As the driving force behind the solutions we’re constantly developing, our people are a force for good in patients’ lives and healthcare business operations. We lead the way in our industry and are working to make the healthcare system more modern and effective. ...

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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 BI Consultant to strengthen the IQVIA Business Intelligence and Data Science team. But wait; Are you up for the challenge; To change the world where you live in? To have an impact on life? To have an impact on the way how pharmaceutic ...

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📑 We are looking for a senior BI Consultant (focus back-end) to strengthen the IQVIA Business Intelligence and Data Science team. But wait; Are you up for the challenge; To change the world where you live in? To have an impact on life? To have an impact on ...

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📑 As a **Project Support & Events Coordinator** you hold a central position in the **Business Analytics and Strategy** (BAS) department of IQVIA Belgium. You will be sharing your time between the **MTOUCH** team (a division of BAS) and the BAS team. Within MTOUCH, you are responsible for the coordination and execution of different types of eve ...

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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 ...

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📑 **Join** **a great team of young & smart talents** **!** We are looking for a **Business Analyst** to join a team of data-driven consultants, being part of the main services/consultancy provider dedicated to the Healthcare Industry. In the commercial services, we partner with business intelligence managers ...

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📑 Job Overview The Senior Project Manager (SPM) role oversees the execution of our Clinical eSource Solution (‘ClinSpark’) implementation projects at customer Early Phase sites, ensuring delivery to customer expectations, to agreed timelines and within budget. The SPM is required to work with highly complex global multi-function c ...

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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.• ...

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📑 We are seeking a talented and motivated health scientist to join our team in Zaventem. In this role, you will have the opportunity to contribute to the development and execution of reimbursement dossiers and value-based healthcare initiatives. We are particularly interested in attracting junior professionals who are starting their career or have mo ...

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📑 As a consultant at Omni Care Consult, you will work on challenging projects that address the issues facing healthcare institutions today. You will deal with complex exercises specific to the sector. Individually or together with your team, you will work on a project basis for various hospitals where you are responsible for the follow-up and result ...

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📑 Join a great team to drive healthcare forward! The Vaccine solution team consists of enthusiastic consulting professionals withdeep expertise & significant experience in the vaccine domain. Our mission is tobringthebroad& depth of vaccine knowledgetoour corporate consulting organisation in order tobetter serve ...

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📑 QVIA is a worldwide top 10 Fortune 500 company, active in Life Sciences. With the merger of Quintiles and IMS Health, IQVIA combines clinical research with a broader use of health data and technology. IQVIA’s data and technology are increasingly used for answering socially relevant questions related to healthcare efficiency, quality and accessi ...

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📑 Head of Regulatory Affairs Benelux Aspen Pharma Group 2023-07-07 Belgium Job Ref #: AP-4195 Industry: Pharmaceutical And Medical/Healthcare Job Type: Permanent Positions Available: 1 Applications are invited for the above indicated vacancy t ...

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📑 Responsibilities As a Associate Regulatory Site Officer you are responsible for managing and reviewing of CMC (Chemistry, Manufacturing and Controls) dossiers, variations, renewals, annual reports, site registrations and territory extensions as part of regulatory product lifecycle management responsibility ...

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📑 Regulatory Affairs Officer Global Registrations Animal Health Human Health Contract Manufacturing Belgium Over KELA KELA, opgericht in , is een Belgische farmaceutische bedrijvengroep. KELA is een betrouwbare ontwikkelaar, producent en verdeler van veterinaire ...

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📑 You manage the regulatory activities for a diverse range of products, including but not limited to: prepare, submit and follow-up regulatory submissions (BLA, CTD, NDA,…), assess post-approval changes, manage responses to the Board of Health, review of packaging/inserts… You collaborate closely with the Regulatory Affairs team and o ...

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📑 About the job We are seeking for a Regulatory Affairs Officer/Specialist responsible for ensuring the delivery of regulatory activities performed on the Benelux market. About us Group 10 Responsibilities Ensure that the regulatory tasks and functions within the Regulato ...

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📑 Job Description: Responsibilities: Regulatory intelligence: Keep track of and evaluate regulatory updates, legislative changes, and industry-specific guidelines related to chemicals.Risk Assessment: Determine the impact of regulatory changes on the organization's operations, products, and se ...

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📑 Job Description Keyrus Life Science is looking on a regular basis for Regulatory Affairs Consultants to join our consulting team for clients (from big pharma to small biotech) projects based in Belgium. This job description is an example on how your job could look like. Once we have a specifi ...

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📑 For our Diabetes Care division, we are recruiting a Senior Regulatory Specialist for Benelux. The Senior Regulatory Specialist is responsible for managing an efficient program to ensure that all regulatory activities for Abbott Diabetes Care products are achieved to an agreed schedule. Role and Responsibilities ...

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📑 A leading firm in the oncology research sector is in search of a Manager, Statistical Programming. This pivotal role is centred around managing statistical vendor deliverables, boosting data quality for regulatory submissions, and pioneering oncology programming standards, contributing significantly to the progression of cancer treatment resear ...

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📑 Are you passionate about Financial Crime with an eagle eye for detail? Do you love interpreting regulatory and legislative requirements to establish policies and procedures that protect us and our customers? Apply now and join us! In this role, you’ll work with Euroclear colleagues in departments across our business on a daily basis pro ...

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📑 Job Description Keyrus Life Science is looking on a regular basis for Technical Regulatory CMC Writers to join our consulting team for clients (from big pharma to small biotech) based in Belgium . This job description is an example on how your job could look like. Once we have a spec ...

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📑 Eames is working exclusively with a global insurance carrier on a Compliance Manager appointment for their newly established Belgium office. The individual will lead our client's Belgian Compliance function, providing oversight of regulatory risk and establishing fit for purpose procedures and guidelines. Core Responsibilities: ...

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📑 Regulatory Affairs Associate - 2407017279W **Description** Kenvue is currently recruiting for: **Regulatory Affairs Associate** This position reports to the Head Of Regulatory Affairs Benelux and is based in Antwerp (Belgium). **Who we are** At Kenvue ( , we realize the ...

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📑 As a Senior Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. As a Senior Medical Writer you will be supporting a Top-5 pharma company. You have the chance to help our customer to deliver best-in-class regulatory and submission documents. While ...

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📑 Who Are We? Toro Europe, located in Oevel-Westerlo Belgium, acts as the European Distribution Center for all equipment related to green maintenance. We are a subsidiary of The Toro Company which is a homegrown, Minnesota-based company that has been in business since 1914. We pride ourselves on providing world class equipment to ...

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📑 Job Description Our client is a global leader in non-invasive neurosurgical treatments. The company is dedicated to improving patient lives by collaborating with physicians, medical institutions, academic researchers and regulatory bodies around the world. They are currently looking for a Sales & Marketing M ...

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📑 Who Are We? Toro Europe, located in Oevel-Westerlo Belgium, acts as the European Distribution Center for all equipment related to green maintenance. We are a subsidiary of The Toro Company which is a homegrown, Minnesota-based company that has been in business since 1914. We pride ourselves on providing worl ...

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