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📑 Make 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, work at pace and challenge perceptions. That’s wh ...

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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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📑 Make 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, work at pace and challenge perceptions. That’s wh ...

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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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📑 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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📑 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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📑 Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology ...

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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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📑 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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📑 **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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📑 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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📑 Manager QA PV Auditor - 2406183539W **Description** At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promis ...

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📑 Role Overview We are currently looking for a Head of Regulatory Affairs and Pharmacovigilance to join a leading Pharmaceutical company based in the Kent area. As the Head of Regulatory Affairs and Pharmacovigilance you will be responsible for providing organisation with strategic advice for the launch of new products in EU & UK. Key Duti ...

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📑 Medical Science Liaison Rheumatology, Scotland & Ireland Location: Scotland / Ireland Salary: Competitive Benefits: Car allowance, bonus, pension, healthcare, We are looking for an experienced MSL to join an excellent, growing Global Medium Sized Pharma company. Internal development prospects, great package and ...

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📑 Role Overview We are currently looking for a Head of Regulatory Affairs and Pharmacovigilance to join a leading Pharmaceutical company based in the Kent area. As the Head of Regulatory Affairs and Pharmacovigilance you will be responsible for providing organisation with strategic advice for the launch of new products in E ...

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📑 Overview At Kyowa Kirin International (KKI), our purpose is to make people smile. This means more than drug discovery and development; it is about embedding care into everything we do to make a difference every day for those that need it most. We’re an inclusive pharmaceutical company that takes time to understand what really matters to our ...

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📑 Job DescriptionReporting to Associate Director, Medical Safety Surveillance.Homebased role available in UK, Spain or US.Comprehensive salary, bonus and benefits package. Role overview:The Affiliate PV Partner Compliance Specialist supports the establishment and maintenance of effective compliance & oversight of external providers of pharmacovigilan ...

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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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📑 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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📑 Overview At Kyowa Kirin International (KKI), our purpose is to make people smile. This means more than drug discovery and development; it is about embedding care into everything we do to make a difference every day for those that need it most. We’re an inclusive pharmaceutical company that takes time to understand wha ...

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📑 Pharmacovigilance Scientists - Associate Director/ Director/ Senior Director Positions in GSK Safety Evaluation and Risk Management (SERM) - Specialty Safety Business. Exciting opportunities to make a significant impact on patients’ lives Provides in-depth medical/scientific expertise in the safety evaluation and risk management of ke ...

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📑 Job DescriptionReporting to Associate Director, Medical Safety Surveillance.Homebased role available in UK, Spain or US.Comprehensive salary, bonus and benefits package. Role overview:The Affiliate PV Partner Compliance Specialist supports the establishment and maintenanc ...

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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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📑 Brief Description: To lead Jazz’s Pharmacovigilance QA (GvP) function to assure regulatory compliance and data integrity in all Jazz activities related to Pharmacovigilance. Essential Functions In collaboration with the Sr Dir, Clinical & PV QA, ensures the implementation of the Global Quality strategy, as relevant to pharmacovigilance (P ...

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📑 Description : Serves as a senior scientific and clinical expert for safety profile of products in therapeutic areas Defines global product safety strategy and routinely manages and leads functional and cross-functional projects Works under consultative direction towards long-term GLPS goals and objectives; assignments are self-initiated wit ...

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📑 Your Job Manage own sales territory (combination of named accounts and/or geographic/market based territory) and achieve annual and quarterly signings and revenue target quotas. Generate new clients through cold calling, networking, business partnerships and sales activity to promote PharmaLex services. </l ...

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📑 Pharmacovigilance Scientists - Associate Director/ Director/ Senior Director Positions in GSK Safety Evaluation and Risk Management (SERM) - Specialty Safety Business. Exciting opportunities to make a significant impact on patients’ lives Provides in-depth medical/scientific expertis ...

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📑 Job Description Excellent opportunity to join a leading pharma company as a Senior Manager - Global Quality Management. The main task is to manage and perform audits with focus on Pharmacovigilance audits. Additional tasks are to support the continuous improvement of Quality System, the inspection management, the regulatory intelligence activiti ...

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📑 Your mission Promote products from the portfolio to all stakeholders in the field of personal care, from presenting products to the possible integration of the sales transaction, and/or by adopting remote promotional techniques in compliance with ethical rules - Make sales calls to healthcare professionals either ...

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📑 MSL - small PharmaLocation: midlands/north of EnglandSalary: CompetitiveBenefits: Car allowance, bonus, shares, pension, healthcareReference: JO-2404-532820An exciting small Pharma business are seeking an experienced MSL to come on board and join their mission in ground breaking science. This business is a few years into their story in the UK and a ...

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📑 MSL - small PharmaLocation: midlands/north of EnglandSalary: CompetitiveBenefits: Car allowance, bonus, shares, pension, healthcareReference: JO-2404-532820An exciting small Pharma business are seeking an experienced MSL to come on board and join their mission in ground breaking science. This business is a few years into their story in the UK and a ...

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📑 Full Stack Mid to Senior Level Software Developer - Fully Remote Available Lead Forensics is a leading SAAS company with products in the B2B sales and marketing space. We’re seeking a mid-level full stack software developer (2+ years' experience) to add to the teams that build our customer facing products. ...

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📑 The ideal candidate for this Account Manager opportunity will come from a biopharmaceutical CDMO background.Candidates can expect to be busy doing a combination of the following:Create value propositions based on customer strategies, technical process, and market insightsDevelop strong strategic relationships within customers’ organisation includin ...

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📑 Brief Description: To lead Jazz’s Pharmacovigilance QA (GvP) function to assure regulatory compliance and data integrity in all Jazz activities related to Pharmacovigilance. Essential Functions In collaboration with the Sr Dir, Clinical & PV QA, ensures the implementation of the Global Quali ...

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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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📑 Job Description Excellent opportunity to join a leading pharma company as a Senior Manager - Global Quality Management. The main task is to manage and perform audits with focus on Pharmacovigilance audits. Additional tasks are to support the continuous improvement of Quality System, the inspection management, the regulatory intelligenc ...

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📑 Role: Global Labelling LeadLocation: United Kingdom - RemoteSalary: Very competitive salary on offerPlanet Pharma are supporting a leading global biotech company with the search for a new Global Labelling Lead to join them during an exciting period of growth! Perfect for someone looking to utilise their skills within an exciting biotech .Role summa ...

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📑 Role: Global Labelling LeadLocation: United Kingdom - RemoteSalary: Very competitive salary on offerPlanet Pharma are supporting a leading global biotech company with the search for a new Global Labelling Lead to join them during an exciting period of growth! Perfect for someone looking to utilise their skills within an exciting biotech .Role summa ...

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📑 About This Job : As we further build our Global Clinical development structure, we have a new opportunity for a Senior Director - Lead Clinical Development Scientist for Immuno- Oncology. The primary focus for this role is the management and input into the development of clinical strategies for assigned modalities or indications within the ...

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📑 About This Job : As we further build our Global Clinical development structure, we have a new opportunity for a Lead Clinical Development Scientist (Senior Director) for Oncology. The primary focus for this role is the management and input into the development of clinical strategies for assigned modalities or indications within the divisio ...

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📑 Our client, based in Dartford, were established in 2011. UK owned they are now expanding and are looking to recruit a Pharmacovigilance Co-ordinator.Job Description: * Develop and approve artwork components and patient information (SPC, PIL, cartons and labelling) and associated mock-ups. * Liaise with project managers for ...

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📑 Excellent opportunity to join a leading pharma company as a Senior Manager - Global Quality Management.The main task is to manage and perform audits with focus on Pharmacovigilance audits. Additional tasks are to support the continuous improvement of Quality System, the inspection management, the regulatory intelligence activities, the SOP and WP m ...

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📑 Excellent opportunity to join a leading pharma company as a Senior Manager - Global Quality Management.The main task is to manage and perform audits with focus on Pharmacovigilance audits. Additional tasks are to support the continuous improvement of Quality System, the inspection management, the regulatory intelligence activities, the SOP and WP m ...

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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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