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Pharmacovigilance information jobs

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Pharmacovigilance Auditor , , UNITED KINGDOM ...audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory Intelligence Provide advice and act as project liaison Skills Degree in natural science or equivalent number of years...
Senior Pharmacovigilance Manager 41680 WEYBRIDGE, SURREY, WEYBRIDGE, SURREY Hobson Prior is seeking a Senior Pharmacovigilance Manager. The successful candidate will maintain the overall safety profiles and any emerging safety concerns concerning the pharmaceutical products. This role is crucial in managing all pharmacovigilance risk management issues and acting as the UK...
Senior Medical Director - CNS/Neurology - Europe - Home-based LONDON, ENGLAND, UNITED KINGDOM ...course of the trial. Pharmacovigilance activity for adverse event analyses and reporting and a medical writing group are integral part of the service offering. Medical Affairs also partner with other functional groups within the Worldwide organization, the generation of statistical and clinical...
Looking for Pharmacovigilance Information jobs? Top Salaries! Full time, part time and contract. Visit PerfectJobs4U UK for the widest selection of top UK jobs. Full time, part time and work from home roles.
Pharmacovigilance Auditor UNITED KINGDOM, UNITED KINGDOM ...audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory Intelligence Provide advice and act as project liaison Skills Degree in natural science or equivalent number of years...
Head of Global Safety Data Integration and Literature (UK) £80 - 100 SLOUGH ...team in the Product Pharmacovigilance & Device Safety team, ideally based in our Raleigh (US), Monheim (Germany), Slough (UK) or Brussels (Belgium) offices. /p p b About the role: /b /p p You will play a pivotal role in oversight and implementation of new and improved solutions to...
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Qualified Person, Pharmacovigilance (QPPV) LUTON, ENGLAND, UNITED KINGDOM ...maintain the company's Pharmacovigilance system. Being the main point of contact for MHRA competent authority. Responsibilities: Acting as the single point of contact for MHRA competent authority on a 24-hour basis. Ensuring the structure and performance of the pharmacovigilance system complies...
Pharmacovigilance Director of Projects (Europe, USA or Canada) , , UNITED KINGDOM We are PrimeVigilance (part of Ergomed PLC), a specialized mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information...
Director, Pharmacovigilance Case Processing UNITED KINGDOM, , UNITED KINGDOM ...quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. Director, Pharmacovigilance (PV) Case Processing...
Multilingual Medical Information Specialist - Norwegian Speaking UNITED KINGDOM, , UNITED KINGDOM ...quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. The Multilingual Medical Information Specialist...
Medical Information Specialist - German Speaking , , UNITED KINGDOM Job Title: Medical Information Specialist - German Speaking Location : Remote (based in UK) Salary: Competitive Job Description Planet Pharma are currently partnered with a leading global Research Consulting Organization providing services to the Pharmaceutical, Medical Device and Biotechnology...
Senior Safety Physician UNITED KINGDOM, , UNITED KINGDOM ...extensive knowledge of pharmacovigilance (PV) legislation to contribute to our team. We are looking for an individual who excels in analytical thinking, can navigate complex data, establish structured processes, and effectively communicate information across our global team. Responsibilities...
Quality Specialist UNITED KINGDOM, , UNITED KINGDOM ...quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. The Opportunity The Quality Specialist position...
Quality & Technical Manager , , UNITED KINGDOM ...SOPs Manage Medical Information Service provider & respond to MI enquiries where required. Preparation, management and review of technical agreements and safety data exchange (PV) agreements Liaise with Marketing Authorisation holders with respect to pharmacovigilance responsibilities. Report...
Regulatory Affairs Manager- Alvita WOKING, ENGLAND, UNITED KINGDOM ...respond to requests for information from national competent authorities. You will be responsible for becoming the subject matter expert on medical devices within the business and ensuring plans are in place to maintain compliance with the requirements of the Medical Devices Regulation (EU...
Director, Drug Safety Lead , , UNITED KINGDOM ...clinical safety and pharmacovigilance support to medicines across life cycle. Reporting to the Head of Drug Safety, this key role will lead the clinical safety activities for the assigned compounds within the organization. You will be accountable for the implementation, execution, and...
Senior Regulatory Affairs Officer , , UNITED KINGDOM ...safety, and product information modifications. Your expertise will be instrumental in writing, compiling, and publishing dossiers for UK National & EU submissions, ensuring compliance with regulatory requirements. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Regulatory Affairs Manager...
Technical Support Analyst UNITED KINGDOM, , UNITED KINGDOM ...Content and Regulatory Information Management technology for regulated industries globally. ISO 27001 accredited, eight of the top 10 global life sciences companies rely on Generis flagship Intelligent Content Services platform, CARA for critical document and information management, including...
Senior Manager, Quality ABINGTON PIGOTTS, ENGLAND, UNITED KINGDOM ...Data Management, Pharmacovigilance, etc.) based on analysis and interpretation of applicable regulations. Identify and partner with key collaborator functions and business partners as appropriate. Assist development team business partners with development and documentation of CAPAs and...
Complaints Intake Analyst , , UNITED KINGDOM ...activities for missing information, coordinating the logistics of complaint sample returns and communicating the results of the complaint investigations when requested/required. Communication and cooperation with customers and distributors involved in the reported complaints Internal...
! RBDS Supervisor based in Andover - Leading Chemical manufacturing! , , UNITED KINGDOM ...ensure correct account information is in place Customer visits for long term contract review meeting Management of office support personnel to ensure technical/service reports for customers Hosting customer audits/visits Enabling service delivery through problem solving Representing the interests...
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