Medical Information Associate

hace 7 días


Buenos Aires, Buenos Aires C.F., Argentina IQVIA LLC A tiempo completo
Job Summary:

We are seeking a highly organized and detail-oriented individual to join our team as an Adverse Event Intake Coordinator. In this role, you will be responsible for managing adverse event reports, collaborating with cross-functional teams, and ensuring regulatory compliance.

Key Accountabilities:
  • Manage and process incoming AE reports, ensuring timely and accurate completion.
  • Collaborate with medical professionals and regulatory agencies to resolve AE cases.
  • Develop and implement procedures for maintaining accurate and complete AE data.
  • Prepare and submit safety reports to regulatory agencies.
Qualifications:
  • Bachelor's degree in a life science field or equivalent experience.
  • Excellent written and verbal communication skills.
  • Proficiency in Microsoft Office Suite.
  • Experience in pharmacovigilance or a related field preferred.


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