Pharmacovigilance Specialist I

Glaukos Corporation
San Clemente, CA
Job Description
This Pharmacovigilance Specialist I role involves processing adverse event information for various study cases, ensuring regulatory compliance, and supporting global pharmacovigilance activities. The position requires a high-level individual with a strong safety-related background and the ability to perform at speed in a fast-paced environment. The role is focused on post-market and clinical trial PV case processing.

Requirements

  • Process adverse event information
  • Ensure regulatory compliance
  • Review ICSRs and assess for regulatory reporting
  • Collaborate with cross-functional teams
  • Assist in safety and risk management activities
  • Adhere to FDA requirements
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