📑 The Recruitment Co are recruiting for an experienced Clinical Trials Manager to join our clients expanding team. A world-leading manufacturer of high-quality technical products.Contract: PermanentSalary: £45,000paShifts: Full timeThe Role: Responsible for all aspects of clinical trial management. The post holder will have a significant level of res ...
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📑 Precision for Medicine (CRO) are recruiting a Regulatory Manager to join our team, candidates can be based in the following countries: UK, Spain, Hungary, Slovakia, Serbia, Romania or Poland.The Regulatory Manager (RM) provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, ...
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📑 Senior Director of Statistics - United Kingdom - Hybrid / Remote - Excellent Remuneration & BenefitsOVERVIEW: I am working exclusively for a SME biotech who are looking for a Director of Biostatistics (Senior also considered) to join as a senior member of a cross-functional asset team, reporting to the Chief Development Officer (CDO). You will cont ...
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📑 Senior Director of Statistics - United Kingdom - Hybrid / Remote - Excellent Remuneration & BenefitsOVERVIEW: I am working exclusively for a SME biotech who are looking for a Director of Biostatistics (Senior also considered) to join as a senior member of a cross-functional asset team, reporting to the Chief Development Officer (CDO). You will cont ...
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📑 Head of Biostatistics - UK/Remote About the role: I have recently partnered with a clinical stage, fast growing Biopharma company who are focused on developing immuno-oncology treatments and other therapies for cancer. In this position you will contribute to the development of compounds within the oncology therapeutic area and drive the design of i ...
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📑 Head of Biostatistics - UK/Remote About the role: I have recently partnered with a clinical stage, fast growing Biopharma company who are focused on developing immuno-oncology treatments and other therapies for cancer. In this position you will contribute to the development of compounds within the oncology therapeutic area and drive the design of i ...
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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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📑 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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📑 We’re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid.The Role:Deliver CTA regulatory strategies and operations for a designated port ...
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📑 We’re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid.The Role:Deliver CTA regulatory strategies and operations for a designated port ...
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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 ...
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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 ...
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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 ...
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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 ...
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📑 BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: ...
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📑 We’re excited to be moving to our vibrant new home on New Oxford Street in central London from the end of June 2024. At GSK HQ, we’re building an energising space where we can connect, collaborate and get ahead of disease together. Designed especially for us, it’ll be one of the healthiest workplaces in the world, with best-in-class tech and bright ...
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📑 Smart Solutions are working with an award winning manufacturer based in Swansea. We are seeking for an enthusiastic experienced Clinical Trials Manager to join our Clinical and Application Research department. You will be responsible for all aspects of clinical trial management. The post holder will have a significant level of responsibility. Dutie ...
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📑 Smart Solutions are working with an award winning manufacturer based in Swansea. We are seeking for an enthusiastic experienced Clinical Trials Manager to join our Clinical and Application Research department. You will be responsible for all aspects of clinical trial management. The post holder will have a significant level of responsibility. Dutie ...
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📑 Smart Solutions are working with an award winning manufacturer based in Swansea. We are seeking for an enthusiastic experienced Clinical Trials Manager to join our Clinical and Application Research department. You will be responsible for all aspects of clinical trial management. The post holder will have a significant level of responsibility. Dutie ...
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📑 Smart Solutions are working with an award winning manufacturer based in Swansea. We are seeking for an enthusiastic experienced Clinical Trials Manager to join our Clinical and Application Research department. You will be responsible for all aspects of clinical trial management. The post holder will have a significant level of responsibility. Dutie ...
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📑 The Recruitment Co are recruiting for an experienced Clinical Trials Manager to join our clients expanding team. A world-leading manufacturer of high-quality technical products. Contract: Permanent Salary: £45,000pa Shifts: Full time The Role: Responsible for all aspects of clinical trial management. The post holder will have a significa ...
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📑 At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development. A Principal Biostatistician with a passion ...
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📑 The Recruitment Co are recruiting for an experienced Clinical Trials Manager to join our clients expanding team. A world-leading manufacturer of high-quality technical products.Contract: PermanentSalary: £45,000paShifts: Full timeThe Role: Responsible for all aspects of clinical trial management. The post holder will have a significant level of res ...
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📑 1,800+ associates. 86 countries. One Regulatory Affairs. At Novartis your voice, experience, and quality mindset can truly make a difference in Regulatory Affairs (RA). Novartis has a unique and promising portfolio with 70 projects as potential NMEs in development, 65 projects in Phase 3 or already undergoing registration, and 100 Phase 1/2 project ...
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📑 The Recruitment Co are recruiting for an experienced Clinical Trials Manager to join our clients expanding team. A world-leading manufacturer of high-quality technical products. Contract: Permanent Salary: £45,000pa Shifts: Full time The Role: Responsible for all aspects of clinical tri ...
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📑 Principal Statistical Programmer | Pharma | UK | Home Based |Warman O’Brien are working with a Global Pharma who due to continued success and growth in the UK, have several opportunities for experienced Senior and Principal Statistical Programmers to join them. This is an exciting time to join this inspiring place to work where you will get the cha ...
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📑 Principal Statistical Programmer | Pharma | UK | Home Based |Warman O’Brien are working with a Global Pharma who due to continued success and growth in the UK, have several opportunities for experienced Senior and Principal Statistical Programmers to join them. This is an exciting time to join this inspiring place to work where you will get the cha ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...
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📑 The Recruitment Co are recruiting for an experienced Clinical Trials Manager to join our clients expanding team. A world-leading manufacturer of high-quality technical products.Contract: PermanentSalary: £45,000paShifts: Full time<span style=text-decoration: un ...
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📑 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 goals while taking science ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...
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📑 Description : Senior Project Manager The Senior Project Manager provides management and leadership to plan, prepare, and execute multiple complex and high profile projects. Internally, the Senior Project Manager interfaces with clinical monitoring and site management, clinical data management, SAS pro ...
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📑 Overall job purpose:1.Creating and disseminating relevant trial documentation or document templates2.Primary point of contact for trial specific issues and trial deliverables3.Lead data management activities.Background:We are looking for an enthusiastic experienced Clinical Trials Manager to join our Clinical and Application Research department. Yo ...
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📑 Job Introduction Thanks for checking out our vacancy, we’re delighted you want to learn more about Dechra! Dechra is a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veter ...
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📑 When our values align, there's no limit to what we can achieve. Parexel FSP is currently looking for a Clinical Operations Manager (Regulatory) to join our expanding team in the UK. This will be a home-based position. Working at Parexel offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors ...
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📑 We are currently seeking a talented and experienced Senior Regulatory Affairs Manager to join our client's team in Surrey. Our client is an established cosmetics/pharmaceuticals company looking for someone with expertise in global cosmetic regulations. In collaboration with a highly skilled international team you will help to manage the ...
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📑 100,000+ That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medici ...
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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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📑 At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to m ...
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📑 Overall job purpose:1.Creating and disseminating relevant trial documentation or document templates2.Primary point of contact for trial specific issues and trial deliverables3.Lead data management activities.Background:We are looking for an enthusiastic experienced C ...
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📑 When our values align, there's no limit to what we can achieve. Parexel FSP is currently looking for a Clinical Operations Manager (Regulatory) to join our expanding team in the UK. This will be a home-based position. Working at Parexel offers tremendous long-term job security and prospects. We unde ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...
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📑 Oxford Global Resources is hiring a Clinical Study Lead (IVD experience is a must) for temporary maternity leave. As a Clinical Study Lead/Trial Manager you will be responsible for the development and execution of all study associated documentation including protocols, investigator brochure, informed consent, contracts, and reports, in compliance w ...
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📑 Oxford Global Resources is hiring a Clinical Study Lead (IVD experience is a must) for temporary maternity leave. As a Clinical Study Lead/Trial Manager you will be responsible for the development and execution of all study associated documentation including protocols, investigator brochure, informed consent, contracts, and reports, in compliance w ...
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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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📑 Our client, a leading cell therapy company dedicated to delivering life-saving treatments, is seeking a Medical Director of Hematology/Oncology to oversee clinical trials. With a focus on providing patients with highly effective therapies, our client boasts a robust pipeline and a commitment to innovation in the field of oncology.Responsibilities:P ...
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📑 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 goals while taking science a s ...
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📑 Avania are hiring - Project ManagerWe are currently looking for a Project Manager. Would you like to enhance your career and be an integral part of our passionate, supportive and dedicated team?As the Project Manager, you will have the opportunity to provide leadership through planning, organizing ...
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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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📑 100,000+ That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medici ...
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