Job Description
Duties and Responsibilities:
- Code and enter information into the Product Safety database for Adverse Events reported in association with client’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 SOPs.
Requirements:
- Bachelor’s Degree Required.
- 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.