📑 OUR COMPANY We, at RegASK are a high growth global RegTech company leveraging technology and global network of experts to revolutionize regulatory intelligence, serving the LifeSciences (MedTech, CROs, Pharma) and FMCG industries (Food, Personal Care). RegASK team is highly diverse with more than 10 nationalities across 3 continents, entrepren ...
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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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📑 Regulatory Affairs Manager – Leading Pharma Specialist Medicines – Manchester (hybrid working) - £competitive salary, 10% bonus, pension + other benefits.Please note: This role is a 12month FTC to cover maternity leave. You'll be a permanent member of staff, with a salary/company benefits, for the 12 months. This is not an hourly/daily rate contrac ...
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📑 Regulatory Affairs Manager – Leading Pharma Specialist Medicines – Manchester (hybrid working) - £competitive salary, 10% bonus, pension + other benefits.Please note: This role is a 12month FTC to cover maternity leave. You'll be a permanent member of staff, with a salary/company benefits, for the 12 months. This is not an hourly/daily rate contrac ...
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📑 Job title: Associate Director, Regulatory Affairs A Pharmaceutical business in London is looking for an Associate Director, Regulatory Affairs to join their Global team. In this role you will provide strategic regulatory and scientific assessment on preclinical requirements, and clinical development plans to bring new products to patients in the mo ...
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📑 Job title: Associate Director, Regulatory Affairs A Pharmaceutical business in London is looking for an Associate Director, Regulatory Affairs to join their Global team. In this role you will provide strategic regulatory and scientific assessment on preclinical requirements, and clinical development plans to bring new products to patients in the mo ...
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📑 *OPPORTUNITY TO RELOCATE TO DUBAI, EARN TAX FREE BASE AND COMMISSION SALARYLife Science Recruitment Consultant / US & Global Market Office based in the Marina area of DubaI, UAEOpportunity for an experienced 360 life science market recruiter to join a Dubai based business at Associate / Recruitment Consultant / Senior Recruitment Consultant level. ...
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📑 *OPPORTUNITY TO RELOCATE TO DUBAI, EARN TAX FREE BASE AND COMMISSION SALARYLife Science Recruitment Consultant / US & Global Market Office based in the Marina area of DubaI, UAEOpportunity for an experienced 360 life science market recruiter to join a Dubai based business at Associate / Recruitment Consultant / Senior Recruitment Consultant level. ...
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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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📑 When our values align, there's no limit to what we can achieve. We are currently seeking Regulatory Affairs Professionals with experience in Clinical Trial Applications (CTAs) under the EU-CTR directive. Join our team or work on dedicated client projects as a Senior Regulatory Affairs Consultant, Regulatory Affairs Consultant or Regulatory ...
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📑 Planet Pharma are currently partnered with a top 10 pharmaceutical company who are seeking a External Data Manager to join the external data team and oversee and support the day to day operations of the company’s drug portfolio. This is a home based position with HQ in the UK (However we are open to candidates from Ireland and Netherlands). The cli ...
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📑 Planet Pharma are currently partnered with a top 10 pharmaceutical company who are seeking a External Data Manager to join the external data team and oversee and support the day to day operations of the company’s drug portfolio. This is a home based position with HQ in the UK (However we are open to candidates from Ireland and Netherlands). The cli ...
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📑 Job Title: Medical Information Specialist - German SpeakingLocation: Remote (based in UK)Salary: CompetitiveJob DescriptionPlanet Pharma are currently partnered with a leading global Research Consulting Organization providing services to the Pharmaceutical, Medical Device and Biotechnology industries across the world. Our client is currently seekin ...
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📑 Job Title: Medical Information Specialist - German SpeakingLocation: Remote (based in UK)Salary: CompetitiveJob DescriptionPlanet Pharma are currently partnered with a leading global Research Consulting Organization providing services to the Pharmaceutical, Medical Device and Biotechnology industries across the world. Our client is currently seekin ...
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📑 Role: HR Operations ManagerLocation: Remote (UK)Job Type: Contract / InterimRate: Competitive Hourly RatePlanet Pharma have partnered with a global biotechnology company assistant them with the search for an Interim HR Operations Manager for an initial 12-month homebased project (UK).Role summary: The Human Resources Operations Manager is key to th ...
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📑 Role: HR Operations ManagerLocation: Remote (UK)Job Type: Contract / InterimRate: Competitive Hourly RatePlanet Pharma have partnered with a global biotechnology company assistant them with the search for an Interim HR Operations Manager for an initial 12-month homebased project (UK).Role summary: The Human Resources Operations Manager is key to th ...
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📑 When our values align, there's no limit to what we can achieve. We are currently seeking Regulatory Affairs Professionals with experience in Clinical Trial Applications (CTAs) under the EU-CTR directive. Join our team or work on dedicated client projects as a Senior Regulatory Affairs Consultant, Regulator ...
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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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📑 Role: Regulatory Affairs AssociateLocation: Maidenhead / M4 corridor.Salary: Very competitive salary on offerPlanet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regulat ...
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📑 Role: Regulatory Affairs AssociateLocation: Maidenhead / M4 corridor.Salary: Very competitive salary on offerPlanet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regulat ...
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📑 Our client, an independent pharmaceutical company who manufacture and specialising in generics, have an opportunity for an experienced EU/ UK Regulatory team leader to join their team in Hampshire.As Regulatory Affairs manager, you will:Leading a small team, handling the regulatory activity across a large portfolio of medicine and medical device/ c ...
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📑 Our client, an independent pharmaceutical company who manufacture and specialising in generics, have an opportunity for an experienced EU/ UK Regulatory team leader to join their team in Hampshire.As Regulatory Affairs manager, you will:Leading a small team, handling the regulatory activity across a large portfolio of medicine and medical device/ c ...
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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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📑 Role: Senior Business System Analyst - DevelopmentLocation: United Kingdom - RemoteSalary: Very competitive salary on offerPlanet Pharma are supporting a leading global pharma company with the search for a new Senior Business System Analyst - Development to join them during an exciting period of growth! Perfect for someone looking to progress in an ...
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📑 Role: Senior Business System Analyst - DevelopmentLocation: United Kingdom - RemoteSalary: Very competitive salary on offerPlanet Pharma are supporting a leading global pharma company with the search for a new Senior Business System Analyst - Development to join them during an exciting period of growth! Perfect for someone looking to progress in an ...
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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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📑 JOB TITLE : Senior Regulatory Affairs Specialist LOCATION : Remote/Hybrid WORKING HOURS : 37.5 Hours, Monday to Friday A brighter future awaits you At CooperVision, we are proud to be the global leader in contact lenses. At our innovative sites worldwide, we manufacture and distri ...
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📑 Role: Markets Research and InsightsLocation: SloughType: ContractDuration: 12 months Planet Pharma are partnered with a leading pharmaceutical client who is seeking a Market Research & Insights Partner. The position is a hybrid role with 2 days on site in Slough until December 2024.Key Responsibilities:Planning and leading agreed market research (a ...
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📑 Role: Markets Research and InsightsLocation: SloughType: ContractDuration: 12 months Planet Pharma are partnered with a leading pharmaceutical client who is seeking a Market Research & Insights Partner. The position is a hybrid role with 2 days on site in Slough until December 2024.Key Responsibilities:Planning and leading agreed market research (a ...
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📑 Regulatory Affairs Advisor - Food Manufacturing BusinessCompany: True North Talent RecruitmentLocation: Fully Remote/ Home BasedPosition: Regulatory Affairs Advisor – Fluent in ArabicSalary: 28-38k full benefits package see belowAbout Us: True North Talent is a recruitment company, dedicated to connecting exc ...
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📑 Role: Regulatory Affairs RoleType: ContractLocation: HampshireDuration: 12 MonthWe are currently partnered with a global Pharmaceutical company who are now looking for a regulatory affairs associate to execute the Regulatory Plan/objectives to ensure the success of new product registrations for an initial 12-month-long contract with the likelihood ...
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📑 Role: Regulatory Affairs RoleType: ContractLocation: HampshireDuration: 12 MonthWe are currently partnered with a global Pharmaceutical company who are now looking for a regulatory affairs associate to execute the Regulatory Plan/objectives to ensure the success of new product registrations for an initial 12-month-long contract with the likelihood ...
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📑 Your newpany This is a clinical-stage Biotechpany. Thispany ismitted to ensuring culture is at the forefront of their business. They have just raised their Series A.Your new role Supports thispanies development by developing and overseeing the execution of regulatory strategies in the US/EU and other territories deemed applicable.What you'll need t ...
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📑 Title: Automation Project Manager - Global PharmaLocation: Near WatfordCompany SummaryMy client is a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas.By joining my client, you will be working for an organisation with a human healthcare philosophy, which means that w ...
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📑 Title: Automation Project Manager - Global PharmaLocation: Near WatfordCompany SummaryMy client is a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas.By joining my client, you will be working for an organisation with a human healthcare philosophy, which means that w ...
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📑 Regulatory Affairs Specialist - Lifecycle MaintenanceLocation: RemoteWe are seeking an experienced Regulatory Affairs Specialist to oversee lifecycle maintenance for our mature product portfolio. The successful candidate will manage compliance activities, coordinate with EU member states under the MRP, handle national product regulations, and ensur ...
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📑 Regulatory Affairs Specialist - Lifecycle MaintenanceLocation: RemoteWe are seeking an experienced Regulatory Affairs Specialist to oversee lifecycle maintenance for our mature product portfolio. The successful candidate will manage compliance activities, coordinate with EU member states under the MRP, handle national product regulations, and ensur ...
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📑 Senior Regulatory Affairs Associate £42,000-50,000 plus benefits | Reporting to VP, Pharmaceutical Operations | UK office (Fitzrovia, London) The Simple Pharma Group creates and develops pharmaceutical companies. Its portfolio of companies comprises Simple Pharma and Androlabs. Simple Pharma is the best home for proven pharma products and provid ...
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📑 The Role Provide regulatory support for all activities conducted by the Company including dossier compilation, variations, change impact assessment, scientific advice applications, paediatric investigation plans, PSUR submissions. To manage the generation and maintenance of Registration Dossiers (MAA/CTD) related with the products manufac ...
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📑 ADVANZ PHARMAs product portfolio and pipeline comprises innovative medicines, specialty generics biosimilars, and originator brands. Our products and pipeline cover a broad range of therapeutic areas, including hepatology, gastroenterology, anti-infectives, critical care, endocrinology, CNS, and, more broadly, rare diseases.We can only achieve our ...
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📑 By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowle ...
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📑 Role: Environment, Health and Safety ManagerType: Permanent Location: MiddletonWe are currently working with a leading pharmaceutical and chemical manufacturing company based in Middleton. We currently hired over 20 personnel for this role and are continuing to support this company with their growth Who are in need of a health and safety lead to co ...
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📑 Role: Environment, Health and Safety ManagerType: Permanent Location: MiddletonWe are currently working with a leading pharmaceutical and chemical manufacturing company based in Middleton. We currently hired over 20 personnel for this role and are continuing to support this company with their growth Who are in need of a health and safety lead to co ...
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📑 Your newpany This is a clinical-stage Biotechpany. Thispany ismitted to ensuring culture is at the forefront of their business. They have just raised their Series A.Your new role Supports thispanies development by developing and overseeing the execution of regulatory strategies in the US/EU and other territories d ...
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📑 SummaryOpportunity to join an award winning Pharma. With several decades in the industry, and new acquisitions, this company can offer security and opportunities for growth.Job DescriptionEnsures compliance with regulatory agency regulations and interpretations. Prepares responses to regulatory agencies' questions and other correspondence. Gathers ...
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📑 SummaryOpportunity to join an award winning Pharma. With several decades in the industry, and new acquisitions, this company can offer security and opportunities for growth.Job DescriptionEnsures compliance with regulatory agency regulations and interpretations. Prepares responses to regulatory agencies' questions and other correspondence. Gathers ...
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📑 ADVANZ PHARMAs product portfolio and pipeline comprises innovative medicines, specialty generics biosimilars, and originator brands. Our products and pipeline cover a broad range of therapeutic areas, including hepatology, gastroenterology, anti-infectives, critical care, endocrinology, CNS, and, more broadly, rare diseases.We can only achieve o ...
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