Product Safety Data Coordinator and Coding Associate

Title: Product Safety Data Coordinator and Coding Associate

Contract – Term: 1 year

Bergen County, NJ

Description of Responsibilities:

  • Code and enter information into the Product Safety database for Adverse Events reported in association with Company’s Marketed and investigational products.
  • The individual will be responsible for verifying the accuracy and completeness of information for each adverse event report for which he/she is assigned in
    conjunction with the source documents and ensuring that the activities are performed in a manner consistent with Company’s SOPs.

Requirements:

  • Health Care Professional (with or without previous drug safety experience) or Non-Health Care Professional with previous drug safety experience desired
  • 2-3 year’s minimum experience in medical coding/terminology within a pharmaceutical organization
  • Computer proficiency required, including data entry of adverse event information into standardized electronic databases such as ARISg/ARGUS
  • Strong written and verbal communications are essential
  • Strong attention to detail and accuracy are essential
  • Strong proofreading, editing and reviewing skills are essential
  • Must be able to work independently, and possess problem solving skills, but also know when to seek assistance from manager

    NOTE: Following a successful 3-4 week on-site training, the candidate will be office based M-F (7.5 hours/day) with start time of between 7:30 AM and 8:30 AM.

  • Accepted file types: doc, pdf, txt, docx.