Product Safety Data Coordinator and Coding Associate - REMOTE
ESR Healthcare
Job Description:
09436 Job Title:Product Safety Data Coordinator and Coding Associate - REMOTE Location:Remote Duration:12 Months Job Description: 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 Client 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. Working Place: New Jersey, New Jersey, United States Company : ESR Healthcare
09436 Job Title:Product Safety Data Coordinator and Coding Associate - REMOTE Location:Remote Duration:12 Months Job Description: 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 Client 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. Working Place: New Jersey, New Jersey, United States Company : ESR Healthcare
Vacancy posted 2 days ago
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