📑 Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization ...
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📑 Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization ...
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📑 Key Responsibilities: - Utilise CAPA systems for case processing - Assure compliance with Good Pharmacovigilance practices - Conduct quality checks on processed cases before submission - Liaise with stakeholders such as medical information personnel Qualifications & Skills Required: -Relevant ...
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📑 Taylor Young is Exclusively partnered with a Global Pharmaceutical company that wants a Drug Safety Physician in EUROPE to join their successful, passionate team!My client has extreme core values, resulting in a great work environment and pleasant staff.This role is a Hybrid position for you to have the best of both w ...
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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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📑 Make your mark for patients Position: Head, Global Safety Data Integration and Literature Make your mark for patients: We are seeking an innovative, strong communicator and influencing Head, Global Safety Data Integration and Literature to join our leadership team in the Product Pharmacov ...
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📑 The Role Reporting directly to the Senior Pharmacovigilance Manager within the Clinical Logistics management department Working to ensure that all policies, procedures and operational processes are fully compliant in accordance to MHRA, EMA, GVP and GCP Monitor operational qua ...
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📑 Responsibilities: The Pharmacovigilance & Regulatory Quality Assurance (PVRQA) Lead / PV Auditor is responsible for leading and coordinating the Global PVRQA activities in the respective region (Americas, Asia-Pacific (APAC), European Economic Area (EEA), ECI) under the general direction of the PVRQA Regional Head, to ensure th ...
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📑 Senior Pharmacovigilance Manager – Biopharmaceuticals - Hertfordshire / Remote Our client, a global biopharmaceutical company with plants across Europe and North America is looking for a Senior Pharmacovigilance Manager to join their team in the UK. This is your chance to be part of one of the top players in the fie ...
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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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📑 For Current Gilead Employees and Contractors:</s ...
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📑 For Current Gilead Employees and Contractors:</s ...
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📑 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 As a **UK National Contact for Pharmacovigilance** you will act as local Qualified Person for customers requiring the services for their product. **RESPONSIBILITIES** · Act as the local Qualified Person in accordance with requirements set out in IQVIA Lifecycle Safety Regulatory Intelligence Database (RID).<b ...
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📑 About the company:We are Qinecsa. Trusted partners to global life science companies. We bring together and offer best-in-class pharmacovigilance technology and scientific expertise to connect life science companies to the right safety solutions.Reportum platformOur automated case intake and follow up platform, Reportum, provides a centralized solut ...
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📑 About the company:We are Qinecsa. Trusted partners to global life science companies. We bring together and offer best-in-class pharmacovigilance technology and scientific expertise to connect life science companies to the right safety solutions.Reportum platformOur automated case intake and follow up platform, Reportum, provides a centralized solut ...
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📑 One of our top 10 pharmaceutical clients are seeking statisticians of various seniority to join and support the companies Statistical research. these roles are working directly in the company and is home based in the UK.The roles are at varying levels detailed below(Associate Manager / Manager) :Exposure to R, SAS, or PythonUnderstanding of regulat ...
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📑 One of our top 10 pharmaceutical clients are seeking statisticians of various seniority to join and support the companies Statistical research. these roles are working directly in the company and is home based in the UK.The roles are at varying levels detailed below(Associate Manager / Manager) :Exposure to R, SAS, or PythonUnderstanding of regulat ...
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📑 BioTalent is headhunting for a UK or Germany based Senior (Global) Drug Safety Physician who is fluent or business level professional in both English and French language. The role is remote with the option of office sites (in UK and Germany) to work from. Responsibilities: Lead clinical safety activities for assigned studies, ensuring compliance wi ...
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📑 BioTalent is headhunting for a UK or Germany based Senior (Global) Drug Safety Physician who is fluent or business level professional in both English and French language. The role is remote with the option of office sites (in UK and Germany) to work from. Responsibilities: Lead clinical safety activities for assigned studies, ensuring compliance wi ...
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📑 Location – RemoteOutside IR35Duration – 12 monthsMake a meaningful difference at AstraZeneca!Bring out the best in each other, and yourself, by working together as one.When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, ...
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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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📑 **For Current Gilead Employees and Contractors:** Please log onto your Internal Career Site (~/cacheable-task/2997$2151.htmld#backheader=true) to apply for this job. At Gilead, we’re creating a healthier world for all people. For more ...
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📑 Title: Clinical Trial Manager - Global Pharma - Complex TrialsLocation: LondonDuration: Full TimeSalary: Competitive Based on ExperienceWe’re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial Manager, due to a expanding pipeline within Virology development. You will be apart of significant growth within its pipelin ...
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📑 Title: Clinical Trial Manager - Global Pharma - Complex TrialsLocation: LondonDuration: Full TimeSalary: Competitive Based on ExperienceWe’re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial Manager, due to a expanding pipeline within Virology development. You will be apart of significant growth within its pipelin ...
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📑 We are looking for UK-based senior business lawyers who are qualified in England & Wales with significant in-house experience and at least 10 years PQE.Selling legal services in a way that no-one else does, The Legal Director provides businesses with high-calibre, experienced lawyers on a part-time and/or flexible basis. The Legal Director is ideal ...
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📑 We are looking for UK-based senior business lawyers who are qualified in England & Wales with significant in-house experience and at least 10 years PQE.Selling legal services in a way that no-one else does, The Legal Director provides businesses with high-calibre, experienced lawyers on a part-time and/or flexible basis. The Legal Director is ideal ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de ...
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