Global Quality Manager with Adverse Event Review

5 dni temu


Warszawa, Mazovia, Polska IQVIA Argentina Pełny etat
Key Responsibilities
  • Performing Pharmacovigilance activities per project requirement.
  • Collecting and tracking incoming Adverse Events and endpoint information.
  • Receiving, reviewing and interpreting medical reports.
  • Processing safety data according to applicable regulations, guidelines, Standard Operating Procedures (SOPs) and project requirements.
  • Determining initial/update status of incoming events.
  • Coding Adverse Events and Products, writing narratives, and performing Literature related activities as per internal/project timelines.
  • Ensure to meet quality, productivity, and delivery standards per project requirements.
  • Identify quality problems, if any, and bring them to the attention of senior team members.
  • Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.


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