22/04/2024 | Fulltime | CV-Library | £50,000 - £55,000 / Year We are currently searching for a remote GVP auditor to join an international CRO. The role will be responsible for deliverly of pharmacovigilance services to their clients including glbal pharma and biotech companies. Responsiblities - Prepares and performs audits on behalf of clients and relevant
Save for laterRegister your CV19/04/2024 | Fulltime | London | CV-Library | £70,000 - £80,000 / Year On experience or experience in diagnostics or medical devices. Ideally, you will have operational experience in Regulatory Affairs, Pharmacovigilance, or Medical Affairs, as well as a minimum of 3 years of Business Development or Sales experience selling services. If you lack experience in the aforementioned
Save for laterRegister your CV16/04/2024 | Fulltime | London | CV-LibraryActively participating in and supporting required QMS activities, including complaint and pharmacovigilance reporting. Your Background Degree qualified in life science or equivalent. Experience of working in a relevant hospital sales role and full UK driving license. ABPI qualified – understands the ABPI
Save for laterRegister your CV08/04/2024 | Fulltime | Marlow | CV-LibraryInvolved in the reported complaints Internal communication and cooperation with relevant local or global stakeholders in other departments involved with complaints management within the organization, like affiliate CQA, Medical Information, Regulatory Affairs and Pharmacovigilance Supports more complex
Save for laterRegister your CV03/04/2024 | Fulltime | City of London | CV-Library | £50,000 - £60,000 / Year Machine Learning (ML), and Natural Language Generation (NLG) technologies to improve automation. Work closely with the Director of Pharmacovigilance to implement best practises and adhere to regulatory irements Proven experience in project management, demonstrating expertise in project
Save for laterRegister your CV02/04/2024 | Fulltime | East Kilbride | CV-LibraryAnd presenting skills Lead and work in a team with a sense of responsibility Track record in pharmaceutical regulatory affairs and medical device legislation Regulatory environment in local and international territories Working in or with manufacturing, quality assurance, (pharmacovigilance), marketing
Save for laterRegister your CV27/03/2024 | Fulltime | Maidenhead | CV-Library | £13 - £14 / Hour Processing, from setting up new account - delivery of product. Process product technical complaints, adverse event and medical information calls, including keeping records and completing month end reports to Pharmacovigilance and PTC management teams (when required)Training and Compliance Ensuring all SOP
Save for laterRegister your CV16/04/2024 | Fulltime | Manchester | ACHIEVA Group Limited | £50,000 - £75,000 / Year Products, competitor products and activities in the working area and suggest corresponding actions. Provide complete transparency of sales activities. Actively participate in Organisations elearning courses, training, seminars and meetings for medical representatives. Pharmacovigilance, promptly
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