Patient Safety Specialist

6 days ago


Plainsboro, New Jersey, United States GForce Life Sciences Full time
Job Summary

GForce Life Sciences is seeking a highly skilled Patient Safety Specialist to join our team. As a key member of our pharmacovigilance department, you will be responsible for ensuring the safety and quality of our products.

Key Responsibilities
  • Process and analyze adverse event reports and technical complaints related to our marketed products.
  • Perform data entry and review of adverse events and associated technical complaints, providing feedback to ensure excellent case quality.
  • Handle incoming and outgoing correspondence, including follow-up calls and correspondence.
  • Collect and document information received during outbound follow-up calls.
  • Perform triage, case classification, and case assignment.
  • Handle escalated calls for adverse events and technical complaints.
  • Support the identification of trends and implementation of corrective actions for issues identified during case review.
  • Coordinate configuration requests for the safety and complaint databases.
Requirements
  • Bachelor's degree in a medical or science-related discipline (or equivalent experience).
  • Minimum of 2 years of progressively responsible, relevant pharmacovigilance experience, including MedDRA coding and adverse event identification.
  • Exceptional knowledge of medical and pharmacovigilance terminology.
  • Proficiency in Windows, Microsoft Word, Excel, and Outlook.
  • Experience with a Call Center and Drug Safety database (preferred).
  • Bilingual (Spanish-English) a plus.


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