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📑 Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in ...

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📑 Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in ...

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📑 The Senior Manager, Global Development Quality Management (GCP) acting as a Quality Management Lead (QML) is a key position that will provide mentorship and leadership for all aspects of quality and compliance. The incumbent will engage with key collaborators, build strategic partnerships working and collaborating closely with study teams, relevant ...

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📑 Your new companyAn established global Biotech in the UK is looking for a regulatory oncology expert to join them on a 12- month contract.Your new roleThe Regulatory Affairs Manager will be there to develop and implement regulatory strategies for EU markets for their Oncology portfolio. This will require someone to have both development and post-mar ...

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📑 Reporting to the Global Patient Safety (GPS) Therapeutic Area (TA) Head, the Senior Director, serves as the first point of contact (POC) for all safety related issues for the compound(s) assigned within the therapeutic area (TA). They are the GPS representative on the cross functional Strategic Program Team (SPT) and the Chair of the Safety Managem ...

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📑 Job Title: Patient Engagement Sr Mgr Global Trial Optimization Department: 1467-Global Clinical Trial ServicesSUMMARY:The Senior Manager, Global Trial Optimization (GTO), Patient Engagement will lead program or study level Patient Recruitment and Retention Strategy development to inform the clinical strategy, study protocols and operational plans t ...

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📑 Your newpanyAn established global Biotech in the UK is looking for a regulatory oncology expert to join them on a 12- month contract.Your new roleThe Regulatory Affairs Manager will be there to develop and implement regulatory strategies for EU markets for their Oncology portfolio. This will require someone to have both development and post-marketi ...

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📑 Your newpanyAn established global Biotech in the UK is looking for a regulatory oncology expert to join them on a 12- month contract.Your new roleThe Regulatory Affairs Manager will be there to develop and implement regulatory strategies for EU markets for their Oncology portfolio. This will require someone to have both developme ...

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📑 We are looking to add a new critical reporting directly to the Executive Director of Global Patient Safety (GPS) within our Quality and Compliance Centers of Excellence (CoE). As the GPS Pharmacovigilance Intelligence Leader, you'll become a central figure in ensuring patient safety by navigating the evolving landscape of international pharmaco ...

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📑 The Global Patient Safety (GPS) lead role (Director of GPS) serves as the first point of contact (POC) for all safety related issues for the compound(s) (asset(s)) assigned within the Solid Oncology therapeutic area (TA), and is the GPS representative on the cross functional strategic program team for the compound. The GPS Lead owns the safety stra ...

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📑 The Global Patient Safety (GPS) lead role (Director of GPS) serves as the first point of contact (POC) for all safety related issues for the compound(s) (asset(s)) assigned within the Solid Oncology therapeutic area (TA), and is the GPS representative on the cross functional strategic program team for the compound. The GPS Lead owns the safety stra ...

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📑 If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that read over 10 m ...

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📑 CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months.Company: Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovat ...

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📑 Global Regulatory Affairs – Due Diligence Manager / Senior ManagerYour newpany This US Biotech are looking for a Regulatory Affairs professional with strong Due Diligence experience to join an exciting, high-profile project, this is initially a 6 month contract but has scope for extension. There is the option to be fully remote.<br ...

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📑 Description KEY RESPONSIBILITIES The Senior Director, CMC Regulatory Affairs Policy, Advisory and Intelligence is a recognized expert both inside and outside the business, and is responsible for leading various aspects of internal and external-facing advocacy as applicable to support the Gilead portfolio. This leader will represent the bu ...

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📑 Career CategoryRegulatoryJob DescriptionIf you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve togethe ...

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📑 When our values align, there's no limit to what we can achieve. We are currently seeking Regulatory Affairs Professionals with experience in Clinical Trial Applications (CTAs) under the EU-CTR directive. Join our team or work on dedicated client projects as a Senior Regulatory Affairs Consultant, Regulatory Affairs Consultant or Regulatory ...

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📑 Global Regulatory Affairs – Due Diligence Manager / Senior ManagerYour newpany This US Biotech are looking for a Regulatory Affairs professional with strong Due Diligence experience to join an exciting, high-profile project, this is initially a 6 month contract but has scope for extension. There is the option to be fully remote.Your new role As the ...

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📑 Description KEY RESPONSIBILITIES The Senior Director, CMC Regulatory Affairs Policy, Advisory and Intelligence is a recognized expert both inside and outside the business, and is responsible for leading various aspects of internal and external-facing advocacy as applicable to support the Gilead portfo ...

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📑 When our values align, there's no limit to what we can achieve. We are currently seeking Regulatory Affairs Professionals with experience in Clinical Trial Applications (CTAs) under the EU-CTR directive. Join our team or work on dedicated client projects as a Senior Regulatory Affairs Consultant, Regulator ...

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📑 UK Pharma company vacancy * Oncology product portfolio * Focus on UK & Ireland HTA submissions * Hybrid role – 1/2 days per week within West London HQ * Salary: Up to £95k plus 20% bonus, car allowance and comprehensive benefits packageThis is a new position within the UK & Ireland business unit of a glob ...

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📑 * UK Pharma company vacancy * Oncology product portfolio * Focus on UK & Ireland HTA submissions * Hybrid role – 1/2 days per week within West London HQ * Salary: Up to £95k plus 20% bonus, car allowance and comprehensive benefits packageThis is a new position within the UK & Ireland business unit ...

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📑 SUMMARY: The responsibility of this role is to aid the expansion of Regeneron in international markets. The individual will work alongside the sourcing manager to establish commercial capabilities to support the organization's brands in various exUS local markets. Together, they will work to optimize value, mitigate risks, and ensure quality an ...

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📑 When our values align, there's no limit to what we can achieve. Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role can be office or home based in va ...

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📑 When our values align, there's no limit to what we can achieve. Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role can be office or home based in va ...

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📑 When our values align, there's no limit to what we can achieve. Parexel is seeking highly motivated and experienced individuals for the position a Senior Regulatory Affairs Associate. This role can be home, or office based in various locations in Europe. As part of our team, you will have the opportunity to work within a collaborative enviro ...

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📑 Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s bigg ...

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📑 When our values align, there's no limit to what we can achieve. Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role ...

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📑 When our values align, there's no limit to what we can achieve. Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role ...

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📑 Description We are looking for a driven individual who is passionate about bringing transformational medicines to those in Europe and international countries with continued unmet medical need. This is an exciting opportunity for a Regulatory Affairs Associate Director to join the Gilead Global Regulatory Affairs Oncology team to suppor ...

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📑 When our values align, there's no limit to what we can achieve. When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by somethi ...

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📑 Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight ...

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📑 At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring ...

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📑 Bei Bristol Myers Squibb lassen wir uns von einer einzigen Vision inspirieren - die Veränderung des Lebens von Patienten durch Wissenschaft. In den Bereichen Onkologie, Hämatologie, Immunologie und Herz-Kreislauf-Erkrankungen - und eine der vielfältigsten und vielversprechendsten Pipelines der Branche - trägt jeder unserer leidenschaftlichen Kolleg ...

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📑 An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidan ...

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📑 An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidan ...

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📑 Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?At Amgen, every challenge is an opportunity. And every opportunity brings the potential to change lives. Our shared mission—to serve patients—has driven our status as one of the world’s preeminent biotechnology com ...

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📑 Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?At Amgen, every challenge is an opportunity. And every opportunity brings the potential to change lives. Our shared mission—to serve patients—has driven our status as one of the world’s preeminent biotechnology com ...

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📑 When our values align, there's no limit to what we can achieve. Parexel is seeking highly motivated and experienced individuals for the position a Senior Regulatory Affairs Associate. This role can be home, or office based in various locations in Europe. As part of our team, you will have the opportunity to work wi ...

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📑 Description The Real-World Evidence (RWE) function at Gilead is part of the Clinical Data Sciences (CDS) group within the Clinical Development organization and aims to unlock the power of Real-World Data (RWD) to help transform innovations to life-changing medicines for patients. The Senior Director, RWE innovation methods and external partn ...

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📑 Are you our next Senior Arrears Specialist?Pepper Advantage is one of the leading specialist loan servicing companies in the UK and we are currently looking for a Senior Arrears Specialist with proven experience in customer service, mortgage administration, and delivery of workout solutions to customers experiencing payment difficulties.This is a h ...

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📑 Are you our next Senior Arrears Specialist?Pepper Advantage is one of the leading specialist loan servicing companies in the UK and we are currently looking for a Senior Arrears Specialist with proven experience in customer service, mortgage administration, and delivery of workout solutions to customers experiencing payment difficulties.This is a h ...

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📑 Description We are looking for a driven individual who is passionate about bringing transformational medicines to those in Europe and international countries with continued unmet medical need. This is an exciting opportunity for a Regulatory Affairs Associate Director to join the Gilead Glob ...

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📑 Global Technology Procurement Manager - FTSE100 - Uxbridge (Hybrid) - £80,000-£90,000 + packageA global FTSE100 business seek a strong IT/Technology Procurement Manager to lead large-scale sourcing projects and devise category strategy across IT Infrastructure (Hardware, Cloud, Data Centres).The role sits within an innovative, data ...

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📑 Global Technology Procurement Manager - FTSE100 - Uxbridge (Hybrid) - £80,000-£90,000 + package A global FTSE100 business seek a strong IT/Technology Procurement Manager to lead large-scale sourcing projects and devise category strategy across IT Infrastructure (Hardware, Cloud, Data Centres). The role sits within an innovative, data driven an ...

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📑 Global Technology Procurement Manager - FTSE100 - Uxbridge (Hybrid) - £80,000-£90,000 + package A global FTSE100 business seek a strong IT/Technology Procurement Manager to lead large-scale sourcing projects and devise category strategy across IT Infrastructure (Hardware, Cloud, Data Centres). The role sits within an in ...

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📑 Job summary We have a fantastic opportunity to join the Research and Development department on a secondment/Fixed term contact for 12 months. The post holder will develop, promote, support, manage and monitor the research service and development activity throughout the Trust, collaborating with the Research D ...

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📑 Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that tran ...

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📑 Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that tran ...

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📑 When our values align, there's no limit to what we can achieve. When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development s ...

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