📑 Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!Why IQVIA?Growth potential - clear pathways to success for those who want to grow with usProfessional development - resources that promote your career growth and programs to help you build knowledge and gain skillsWork-life balance - leaders that suppo ...
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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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📑 Director Health Economics West London I'm collaborating with a global pharmaceutical company in search of a HEOR lead to join their UK division as an integral part of the broader Market Access and HEOR network. This role holds significant influence in spearheading economic value propositions for medical solutions throughout the UK & Ireland, ensuri ...
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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 Infectious Disease are welcome to continue to work in their area of experti ...
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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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📑 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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📑 Director Health Economics West London I'm collaborating with a global pharmaceutical company in search of a HEOR lead to join their UK division as an integral part of the broader Market Access and HEOR network. This role holds significant influence in spearheading economic value propositions for medical solutions throughout the UK & Ireland, ensuri ...
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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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📑 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 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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📑 Integrated Care Specialist - CV/Metabolic - North LondonOur client is a family-owned company whose distinctly independent structure means that they are not constrained by the short-term needs of individual shareholders and can focus on the future within long-term strategies of vision and leadership.They have a reputation for providing effective pro ...
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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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📑 Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging / radiopharmaceuticals or / radiation oncology for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators ...
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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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📑 We are currently seeking a Manager, Patient Recruitment to join our team within our Clinical Operations group. We are seeking an experienced patient recruitment professional with a background in clinical research and health communications, to join our growing patient recruitment team and support our growth. Responsibilities Develop unique recrui ...
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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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📑 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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📑 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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📑 Director Health Economics West London I'm collaborating with a global pharmaceutical company in search of a HEOR lead to join their UK division as an integral part of the broader Market Access and HEOR network. This role holds significant influence in spearheading economic value propositions for medical solutions throughout the UK & Ireland, ensuri ...
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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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📑 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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📑 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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📑 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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📑 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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📑 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 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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📑 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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