Responsibilities Include:

  • Selecting and coding adverse events
  • Determine seriousness of AEs, writing/editing case narratives
  • Perform labeling assessments
  • Requesting follow-up information when needed
  • Adhere to regulations, guidelines, Standard Operating Procedures, data entry and writing practices


  • Bachelor’s Degree
  • 4 to 7 years of experience in Quality Assurance and Quality Control
  • HCP is required
  • Drug Safety experience is desired

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