Product Safety Data Coordinator and Coding Associate
Posted
Title: Product Safety Data Coordinator and Coding Associate
Location: 100% remote
Duration: 12+ Months
Pay Range: $23/hr - $26/hr
37.5 hours per week
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 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.
Location: 100% remote
Duration: 12+ Months
Pay Range: $23/hr - $26/hr
37.5 hours per week
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 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.
