Qualified Person Responsible for Pharmacovigilance (QPPV) in the EU and UK (home

The EU QPPV is responsible for: The establishment and maintenance of a system which ensures that information about all suspected adverse reactions which are reported to the personnel of the Company, and to medical representatives, is collected and collated in order to be accessible at least at one point within the Community; Ensuring that any request from the CAs for the provision of additional information necessary for the evaluation of the benefits and risks afforded by a medicinal product is answered fully and promptly; Provision to the CAs, of any other information relevant to the evaluation of the benefits and risks afforded by a medicinal product, including appropriate information on planned post-authorisation safety studies. Being continuously available to CAs in Member States and the Agency and the MAH, ensuring adequate back-up procedures are in place. Having an oversight of the safety aspects of the company’s medicinal products including an overview of medicinal product safety profiles, any emerging safety concerns, any conditions or obligations adopted as part of the marketing authorisations and other commitments relating to safety or the safe use of the products and other relevant finding raised from studies/programmes conducted by the Company. Life-science education background Medicine (human or veterinary) or Pharmacy preferred Solid knowledge of PV system operations and function Strong knowledge of Global Regulations, standards and best practices regarding safe