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Sundheds-job i Storkøbenhavn

Do you want to contribute to the safety and quality of Novo Nordisk clinical development? Do you have the strong pharmacovigilance experience it takes to execute and supervise on the handling of adverse events reported from clinical trials? Would you enjoy being a key player in making sure that global regulatory requirements are met? If yes, you might be the Senior Clinical Safety Professional we are looking for. Read more and apply today for a life-changing career! The position As a Senior Clinical Safety professional, you will be responsible for handling adverse events reported world-wide from ▶Novo Nordisk◀ clinical trials to ensure that global regulatory requirements are met. You should use your medical background to evaluate and process individual case safety reports and it is expected that you can provide guidance to colleagues and relevant stakeholders in all case handling aspects. Your main responsibilities will be focused on:

  • Anticipating the impact of changes to case handling processes on interconnected and related processes.
  • Contributing to the updates of standard operating procedures (SOPs)/working instructions demonstrating independent Subject Matter Expert expertise within the field of case handling.
  • Participation in projects in Global Patient Safety, e.g., contribute to the oversight, support and coordination of outsourcing activities to CRO and ensuring integrations of new molecules in Safety Operations processes.
  • ...