New York Licensed PV Coordinator

A company is looking for a PV Coordinator.

Key Responsibilities

Ensure timely and accurate processing of adverse event reports in compliance with regulations

Conduct investigations and evaluations of adverse events, collaborating with cross-functional teams

Monitor and analyze safety data to identify potential issues and recommend actions

Required Qualifications and Education

Bachelor's degree or equivalent professional experience

2+ years of experience in Pharmacovigilance / Drug Safety within a CRO or Pharma environment

Strong understanding of Good Clinical Practices (GCPs) and global safety reporting regulations

In-depth knowledge of pharmacovigilance regulations and medical terminology

Experience with safety databases, such as ArisG, is a plus