Product Safety Data Coordinator and Coding Associate - REMOTE (1)

Summary

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

Job Description

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