Pharmacovigilance Data Processor

hace 4 días


Buenos Aires, Buenos Aires C.F., Argentina Iqvia Argentina A tiempo completo

About the Role:

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  • We are seeking a highly motivated and detail-oriented Adverse Event Case Intake Processor to join our growing Pharmacovigilance team.
  • In this critical role, you will be responsible for the accurate and timely intake, processing, and tracking of adverse event reports received from various sources.
  • You will play a vital role in ensuring the safety of our products by diligently adhering to regulatory guidelines, internal Standard Operating Procedures (SOPs), and global best practices.

Responsibilities:

  1. Case Intake & Processing:
  • Receive and process adverse event reports from various sources, including emails, faxes, phone calls, and databases.
  • Conduct initial assessment and triage of adverse events to determine seriousness and reportability.
  • Perform data entry and maintain accurate records in safety databases (e.g., Argus, APEX).
Case Follow-Up:
  • Conduct follow-up with reporters to obtain missing information.
  • Track and manage case processing timelines and ensure timely completion of all activities.
Communication & Collaboration:
  • Communicate effectively with internal stakeholders and external parties as needed.
  • Collaborate with the Pharmacovigilance team to ensure efficient case processing and data management.

Requirements:

  • Bachelor's degree in a life science field or equivalent experience.
  • Fluent local language skills and excellent command of English language.
  • 1+ years of experience in pharmacovigilance or a related field preferred.
  • Strong attention to detail and accuracy.
  • Excellent organizational and time-management skills.


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