Aggregate Reports PV Specialist

Vor 6 Tagen


Solothurn, Solothurn, Schweiz Experis Switzerland Vollzeit

As a highly skilled Pharmacovigilance Aggregate Reports Professional at Experis Switzerland, you will play a critical role in managing the processes for all aggregate reports, ensuring high-quality standards of PV documents, and collaborating with cross-functional teams to develop and implement compliant processes.

The successful candidate will serve as a subject matter expert on relevant safety requirements, company policies/procedures related to pharmacovigilance activities, and aggregate reports knowledge. You will support process improvement, implement and maintain processes, and be responsible for the Aggregate Reports Master Schedule and worldwide legislation overview.

This is an exciting opportunity for a Safety Surveillance and Aggregate Reports Leader who can interact collaboratively and effectively in a team environment, represent and speak to processes in cross-Safety and cross-functional forums, and contribute to initiatives for process improvement and consistency regarding aggregate reporting, clinical trial safety oversight, signal management, and responding to ad hoc safety questions.

  • Project management and authoring of aggregate safety reports such as PSURs, DSURs, PADERs, and local reports.
  • Serves as a subject matter expert on relevant safety requirements, company policies/procedures related to pharmacovigilance activities, as well as aggregate reports knowledge.
  • Support process improvement; implement and maintain processes.
  • Responsible for the Aggregate Reports Master Schedule and worldwide legislation overview (production, update, stakeholders review).


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