Job Description

Responsibilities:

  • Responsible for the assessment, management, and submission of adverse event reports in the PV database.

  • Identify issues in case processing that may result in a delay in submission and escalate issues to management as appropriate.

  • Comply with internal and external timelines for managing adverse events and product complaint case processing and case submission processes as appropriate.

  • Validation of data entry against source documents and call notes as appropriate.

  • Attempt to obtain follow-up information from external parties through effective written and oral communications.

    • What You Need to Succeed (minimum qualifications):

  • Strong understanding of medical terms, clinical concepts, and their relevance in adverse event case processing.

  • 4-7 Years of Experience.

    • What will give you a competitive edge (preferred qualifications):<...

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