Product Safety Data Coordinator

Description of Responsibilities:

• Code and enter information into the Product Safety database for Adverse Events reported in association with our 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.

Requirements:

• 2-3 year’s minimum experience in medical coding/terminology within a pharmaceutical organization.
• Strong proofreading, editing and reviewing skills are essential
• Bachelor's Degree required
• Computer proficiency required, including data entry of adverse event information into standardized electronic databases such as ARISg/ARGUS
• Health Care Professional (with or without previous drug safety experience) or non-health Care Professional with previous drug safety experience desired
• Strong attention to detail and accuracy are essential
• Must be able to work independently, and possess problem solving skills, but also know when to seek assistance from manager.
• Strong written and verbal communications are essential