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.