📑 Brief Description: The Senior Manager, Pharmacology Scientist directs, leads, and manages Jazz non-clinical Pharmacology projects from conceptualization and study design through to study report finalization and subsequent scientific publications, and inclusion in regulatory documentation. Manages interactions and collaboration with key stakeh ...
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📑 Brief Description: The Senior Manager, Pharmacology Scientist directs, leads, and manages Jazz non-clinical Pharmacology projects from conceptualization and study design through to study report finalization and subsequent scientific publications, and inclusion in regulatory documentation. Manages interactions and colla ...
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📑 Brief Description: The Director, Medical Communications is responsible for the development of medical publications as well as the management of publication agencies/vendors and the associated budgets, and oversight of internal medical writer led projects. This role collaborates with the medical communication lead for t ...
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📑 Brief Description: The Discovery and Medicinal Chemistry Department at Jazz Pharma is seeking an enthusiastic scientist to join the Preformulation & Biopharmaceutics at the Kent Science Park site in Sittingbourne. You will work together with other CMC scientists to advance drug candidates from lead optimization to proo ...
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📑 Brief Description: The Manager of Quality & Compliance (Q&C) for Pharmacovigilance (PV) is responsible for performing quality assurance activities to ensure that Jazz is adhering to Global applicable regulations, industry standards, Jazz policies, procedures and quality standards in support of the Quality Management System within the Researc ...
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📑 Brief Description: The Manager of Quality & Compliance (Q&C) for Pharmacovigilance (PV) is responsible for performing quality assurance activities to ensure that Jazz is adhering to Global applicable regulations, industry standards, Jazz policies, procedures and quality standards in support of the Quality Management S ...
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📑 Job DescriptionIf you are a Jazz employee please apply via the Internal Career siteJazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with ...
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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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📑 JobDescriptionIf you are a Jazzemployee please apply via the Internal CareersiteJazz Pharmaceuticals plc (NASDAQ: JAZZ) is aglobal biopharmaceutical company whose purpose is to innovate totransform the lives of patients and their families. We arededicated to developing lifechanging medicines for people withserious ...
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📑 Job DescriptionIf you are a Jazz employee please apply via the Internal Career siteJazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limi ...
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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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📑 JobDescriptionIf you are a Jazzemployee please apply via the Internal CareersiteJazz Pharmaceuticals plc (NASDAQ: JAZZ) is aglobal biopharmaceutical company whose purpose is to innovate totransform the lives of patients and their families. We arededicated to developing lifechanging medicines for people withserious diseases often with limited or no ...
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📑 Brief Description: The Senior Manager, Regulatory Information Management (RIM), will work closely with R&D and Manufacturing well as other functions within Jazz, to manage training, documentation, user experience, and maintenance of the RIM system and integration with the other systems at Jazz Essential Functions Understand the business p ...
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📑 Brief Description: The Senior Manager, Regulatory Information Management (RIM), will work closely with R&D and Manufacturing well as other functions within Jazz, to manage training, documentation, user experience, and maintenance of the RIM system and integration with the other systems at Jazz Essential Functions Understand the business p ...
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📑 Brief Description: The Senior Manager, Regulatory Information Management (RIM), will work closely with R&D and Manufacturing well as other functions within Jazz, to manage training, documentation, user experience, and maintenance of the RIM system and integration with the other systems at Jazz Essential Fun ...
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📑 Brief Description: The Senior Manager, Regulatory Information Management (RIM), will work closely with R&D and Manufacturing well as other functions within Jazz, to manage training, documentation, user experience, and maintenance of the RIM system and integration with the other systems at Jazz Essential Fun ...
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📑 Brief Description: This position is part of the global Quality organization. The primary role of the Learning Management System (LMS) Specialist is to support and maintain the LMS data so that training is in compliance with regulations and business needs. This includes triage and action of JazzLearn business requests ( ...
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📑 Overview About Certara Certara accelerates medicines using proprietary biosimulation software, technology and services to transform traditional drug discovery and development. Its clients include more than 2,000 biopharmaceutical companies, academic institutions and regulatory agencies across 62 countries.</ ...
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📑 Brief Description: This position will lead and participate in various types of GCP/GLP compliance audits for Jazz Pharmaceuticals’ development programs including but not limited to, clinical investigator sites, service providers, and internal systems and processes globally. In addition, this position is responsible for supporting regulatory a ...
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📑 Job Title: MES Expert Drug Product Biologics Switzerland Location: Basel area, Switzerland C ompany Overview: Our Drug Product Business Unit, based in the thriving Basel area of Switzerland, presents exciting opportunities for individuals seeking to make a difference in pharmaceutical ...
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📑 Your newpany You will be joining an innovative biopharmaceuticalpany who have an excellent reputation for Research & Development. They have been investing heavily within their Bioinformatics & Data Science capabilities over the last few years and are continuing to expand their teams as well as their technology.They are looking to a ...
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📑 Overview Certara accelerates medicines using proprietary biosimulation software, technology and services to transform traditional drug discovery and development. Its clients include more than 2,000 biopharmaceutical companies, academic institutions and regulatory agencies across 62 countries. Simcyp is part of Certar ...
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📑 If you are a Jazz employee please apply via the Internal Career siteJazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no thera ...
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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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📑 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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📑 Aspiring Music Teacher Program - £36,500 Permanent Contract A fantastic Secondary School in the Borough of Hammersmith & Fulham are on the hunt for Aspiring Music Teacher for a September 2024 start. This is a full time, and permanent post. ** Due to a candidate shortage this year my client is looking to take people on a permanent contract at £36,5 ...
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📑 Brief Description: This position will lead and participate in various types of GCP/GLP compliance audits for Jazz Pharmaceuticals’ development programs including but not limited to, clinical investigator sites, service providers, and internal systems and processes globally. In addition, this position is responsible for ...
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📑 Music Team Booking AgentRonnie Scott’s is looking for an ambitious music booking agent with a background in live music promotion and programming, marketing, and events. This busy, varied, and interesting role will play a pivotal part in the music team at Ronnie Scott’s. The successful candidate must be energetic, ambitious, creative, have an eye fo ...
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📑 Music Team Booking AgentRonnie Scott’s is looking for an ambitious music booking agent with a background in live music promotion and programming, marketing, and events. This busy, varied, and interesting role will play a pivotal part in the music team at Ronnie Scott’s. The successful candidate must be energetic, ambitious, creative, have an eye fo ...
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📑 This might be the opportunity you’ve been waiting for! A leading regulatory consultancy company is seeking a skilled Principal Clinical Consultant to join its dynamic team in the UK. As a Principal Clinical Consultant, you’ll get the chance to provide strategic, technical, and regulatory advice/services to clients in diverse therapeutic areas, ...
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📑 Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a d ...
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📑 Are you ready to further your career by using your expertise as a Pharmacometrician responsible for the conduct of Modeling and Simulation studies? Do you want to be the pivotal point for impactful studies across the drug development process? Do you want to work for a reputable organizati ...
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