Product Safety Data Coordinator and Coding Associate
Posted
Product Safety Data Coordinator and Coding Associate:
This position is within the Product Safety Group.
37.5 hours per week
100% remote
Description of Responsibilities:
Code and enter information into the Product Safety database for Adverse Events
reported in association with 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.
This position is within the Product Safety Group.
37.5 hours per week
100% remote
Description of Responsibilities:
Code and enter information into the Product Safety database for Adverse Events
reported in association with 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.
