Job Details

Product Safety Data Coordinator and Coding Associate
100% Remote/Nutley-NJ (EST Time Hours)
Duration: 12 Months+
This position is within Product Safety Group.
Hours: 37.5 hours per week
100% remote
Shift: 1st Hours- EST

Hiring Manager's Note:
Message Body:
Alzheimer's focused so neuro preferred.
Easy to pivot and move in a different direction
Need pharma speak
Must have at least 1-2 years in pharma

Bachelor's Degree Required.
ARISg/ARGUS Coding software
Terminology: medical dictionary (MedDRA) and drugs using WHO Drug Dictionary
Profile Title: Drug safety/PV only
Coding exp: Min 2-3 year's minimum experience in medical coding/terminology
Health Care Professional is Huge Bonus.

Description of Responsibilities:
Code and enter information into the Product Safety database for Adverse Events reported in association with ***'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 ***'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.

Bachelor's Degree Required.