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📑 Group Audit Manager - Methodologies and Change Employer Location England Salary GBP75000.0 - GBP85000.0 per annum + £75-85000 plus benefits Closing date 14 Mar 2024 View more Sector Salary band , Contract type Hours Where will they be working? You need to or to save a job. Job Details ...

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📑 Group Audit Manager- Methodologies and Change Employer Location England Salary GBP75000.0 - GBP85000.0 per annum + + excellent bens Closing date 20 Mar 2024 Sector Salary band , Hours Where will they be working? You need to or to save a job. Job Details Your new company < ...

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📑 Our cFSP (sponsor dedicated) team are growing; join us on our mission to drive healthcare forward!We are recruiting for a Senior Clinical Research Associate to assist our sponsor’s Early Development team (phase 1).This is a fully remote position (open to candidates anywhere in the UK) with travel to sites.Why IQVIA?Growth potential - clear pathways ...

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📑 Description Clinical Trial Specialist Apprentice Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and ...

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📑 Brand Manager - Respiratory - BerkshireOur client is an innovation led transnational pharmaceutical company producing a wide range of generic and branded formulations. The behaviour of their leadership team and people has created an environment where entrepreneurship and innovation thrive.As part of their continued expansion in the UK, they are now ...

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📑 For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your ski ...

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📑 For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your ski ...

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📑 Senior QA Specialist I am partnered exclusively with an established and fast-growing pharmaceutical contract services provider that has invested significantly into growth over the past 10 years. They are working in a contract manufacturing, packaging and distribution capacity with clients on a global level. Given the success of the company across i ...

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📑 Account Specialist - Respiratory - NottinghamOur client is a privately-owned Company which allows them the freedom to decide which research they invest in. They have a strong code of ethics and conduct and have a commitment to ethical and social responsibility. They have medicines within Cardiovascular, Neonatal, Transplantation, Respiratory, and h ...

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📑 Senior QA Specialist I am partnered exclusively with an established and fast-growing pharmaceutical contract services provider that has invested significantly into growth over the past 10 years. They are working in a contract manufacturing, packaging and distribution capacity with clients on a global level. Given the success of the company across i ...

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📑 Are you a visionary leader with a distinguished career in AI and data science, backed by an advanced degree in Engineering, Computer or Data Science, or a related field? Are you ready to steer the ship towards innovative horizons by overseeing the implementation of large language models (LLMs) for interactive AI applications? If so, we have an exce ...

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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 19,00 ...

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📑 Our clinical activities are growing rapidly, and we are currently seeking a full-time Site Relationship Coordinator to join our vibrant Clinical Operations team in London. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key str ...

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📑 Working in ICON Strategic Solutions is more than a job, it’s a calling for people who care and have passion for improving patients’ lives. It takes courage to move from one job to another and the process involves careful consideration. At ICON, we care about our people as they are the key to our success and provide an open and friendly work environ ...

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📑 Territory Sales Manager - Orthopaedic Implants - North London & East AngliaOur client is an internationally recognised joint replacement devices innovator. They are focused on improving the quality of life of all patients who receive one of their devices.Combining over four decades of passion, knowledge and innovation, they are committed to their r ...

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📑 Territory Sales Manager - Ostomy Care - East Anglia & North LondonOur client is a major player in the Chronic care marketplace, both here in the UK and overseas. They are renowned for some niche products, innovating service offerings and have exciting growth plans for the next few years.They are currently looking for a highly motivated and enthusia ...

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📑 Senior QA Specialist I am partnered exclusively with an established and fast-growing pharmaceutical contract services provider that has invested significantly into growth over the past 10 years. They are working in a contract manufacturing, packaging and distribution capacity with clients on a global level. Given the success of the company across i ...

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📑 Account Specialist - Respiratory - South East LondonOur client is a privately-owned Company which allows them the freedom to decide which research they invest in. They have a strong code of ethics and conduct and have a commitment to ethical and social responsibility. They have medicines within Cardiovascular, Neonatal, Transplantation, Respiratory ...

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📑 Medpace is currently seeking an office or home based Director of Proposals to join our Clinical Operations team at our London office. The Director will collaborate closely with our medical experts and senior functional managers to create the operational strategy for new business development opportunities. This will include direct management of the ...

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📑 Key Account Manager - Urology - NE, NW and NC LondonThis award-winning pharmaceutical organisation was recently voted as one of the Best Companies to Work For due to their very open, people-focused culture and flexible working environment.Their medicines are diverse and include best in class Oncology, Transplantation, Anti-Infective, Urology, Derma ...

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📑 Our European activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Assistant in either London, England or Stirling, Scotland, UK to join our Regulatory Submissions team, supporting two of our key sub- teams within the department: The central labeling team in development of clinical trial labels The regulatory int ...

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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 19,00 ...

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📑 Medpace is currently seeking candidates with CVRM PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in perfor ...

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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 19,00 ...

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📑 Our European activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Assistant in either London, England or Stirling, Scotland, UK to join our Regulatory Submissions team, supporting two of our key sub- teams within the department: The central labeling team in development of clinical trial labels The regulatory int ...

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📑 Position: Project Coordinator Location: Office-based, London Overview: This position will provide extensive training and is suitable for recent graduates; internship, industrial placement, NHS or Clinical Trials experience is also beneficial Due to continuous business growth and a strong study pipeline, we are looking for Project Coordinators to ...

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📑 Working in ICON Strategic Solutions is more than a job, it’s a calling for people who care and have passion for improving patients’ lives. It takes courage to move from one job to another and the process involves careful consideration. At ICON, we care about our people as they are the key to our success and provide an open and friendly work environ ...

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📑 Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in the United Kingdom, specifically in London and Stirling. Clinical Trial Managers with expertise in Neuroscience and CNS are welcome to continue to work in their area of exper ...

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📑 Have you got an interest in science but don't have the educational background or experience?Are you looking for the opportunity to get an insight into working in the scientific field and a large global organisation?If this sounds like what you're looking for, this is the role just for you! About Labcorp: At Labcorp, we are working together to build ...

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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, IQVIA is able to reliev ...

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📑 Senior QA Specialist I am partnered exclusively with an established and fast-growing pharmaceutical contract services provider that has invested significantly into growth over the past 10 years. They are working in a contract manufacturing, packaging and distribution capacity with clients on a global level. Given the success of the company across i ...

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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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📑 Our European activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Assistant in either London, England or Stirling, Scotland, UK to join our Regulatory Submissions team, supporting two of our key sub- teams within the department: The central labeling team in development of clinical trial labels The regulatory int ...

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📑 The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and/or health/life science interest and background who want to explore the research field, travel the UK, ...

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📑 We are currently seeking a Feasibility Coordinator, who will be a member of our global clinical operations team. By working cross functionally with our clinical operations, medical and regulatory submissions team s, researching internal and public domain databases, as well as through obtaining direct feedback from investigative sites, this individu ...

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📑 Our European activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Assistant in either London, England or Stirling, Scotland, UK to join our Regulatory Submissions team, supporting two of our key sub- teams within the department: The central labeling team in development of clinical trial labels The regulatory int ...

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📑 Working in ICON Strategic Solutions is more than a job, it’s a calling for people who care and have passion for improving patients’ lives. It takes courage to move from one job to another and the process involves careful consideration. At ICON, we care about our people as they are the key to our success and provide an open and friendly work environ ...

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📑 Key Account Manager - Gastroenterology & Urology - East of ScotlandOur client's product portfolio demonstrates an exceptionally innovative and successful track record in the fields of Urology, Endocrine Oncology, Gastroenterology, Endocrinology (Growth) and Reproductive Health (Infertility and Obstetrics).The common thread is that the Company remai ...

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📑 Our clinical operations activities are growing rapidly and we are currently seeking full-time, Regulatory Submissions Technical Advisors to join our Site Activation and Maintenance team, within Clinical Operations. This position plays a key role at Medpace, p reparing and reviewing regulatory documents and providing strategic regulatory advice to s ...

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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 19,00 ...

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📑 Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of cli ...

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📑 Responsibilities We are currently seeking a Director, Feasibility, who will be an integral team leader within our global Proposals and Feasibility team. This position will evaluate and support new clinical trial opportunities by working strategically with Medpace Medical Experts, Clinical Trial Managers and our Regulatory Submissions team. By coll ...

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📑 Senior QA Specialist I am partnered exclusively with an established and fast-growing pharmaceutical contract services provider that has invested significantly into growth over the past 10 years. They are working in a contract manufacturing, packaging and distribution capacity with clients on a global level. Given the success of the company across i ...

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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 19,00 ...

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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 pharmacovigi ...

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📑 Our European activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Assistant in either London, England or Stirling, Scotland, UK to join our Regulatory Submissions team, supporting two of our key sub- teams within the department: The central labeling team in development of clinical trial labels The regulatory int ...

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📑 Our European activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Assistant in either London, England or Stirling, Scotland, UK to join our Regulatory Submissions team, supporting two of our key sub- teams within the department: The central labeling team in development of clinical trial labels The regulatory int ...

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📑 Our European activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Assistant in either London, England or Stirling, Scotland, UK to join our Regulatory Submissions team, supporting two of our key sub- teams within the department: The central labeling team in development of clinical trial labels The regulatory int ...

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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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📑 Working in ICON Strategic Solutions is more than a job, it’s a calling for people who care and have passion for improving patients’ lives. It takes courage to move from one job to another and the process involves careful consideration. At ICON, we care about our people as they are the key to our success and provide an open and friendly work environ ...

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