Safety Surveillance Analyst

Vor 4 Tagen


Solothurn, Solothurn, Schweiz TN Switzerland Vollzeit

Are you passionate about pharmacovigilance? Do you have experience in aggregate safety reports writing and safety signal management? If yes, we are looking for a talented individual to join our team as a PV Reporting Expert at TN Switzerland. In this role, you will contribute to initiatives for process improvement and consistency regarding aggregate reporting, clinical trial safety oversight, signal management, and responding to ad hoc safety questions.

Duties and Responsibilities:
  • Develop, implement, and maintain compliant processes with global PV regulations.
  • Manage and author aggregate safety reports such as PSURs, DSURs, PADERs, local reports.
  • Expertise in pharmacovigilance and drug development regulations.
  • Cross-functional collaboration and team leadership skills.


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