Job Description
Description of 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 Client’s SOPs.
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 year’s minimum experience in medical coding/terminology.
- Health Care Professional is Huge Bonus.
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.