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Job Requirements of Product Safety Data Coordinator and Coding Associate:
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Employment Type:
Contractor
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Location:
Nutley, NJ (Onsite)
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Product Safety Data Coordinator and Coding Associate
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:
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 years 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 years 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.