Summary:
Data entry into the Product Safety database for Adverse Events reported in association with Companys Marketed and investigational products.
The activities include, but are not limited to, data entry, coding into standard dictionaries and writing of narratives based on information provided both on standard forms and from medical records and other documents.
The individual will be responsible for verifying the accuracy and completeness of information for each adverse event report for which he/she is responsible in conjunction with the source documents and ensuring that the activities are performed in a manner consistent with Companys SOPs.



Requirements:

Health Care Professional (with or without previous drug safety experience ) or non- health Care Professional with previous drug safety experience desired
Medical terminology understanding required, with proficiency with MedDRA or doing into other standard medical coding dictionary preferred
2-3 years minimum experience in medical coding/terminology/data entry within a pharmaceutical organization
Computer proficiency required, including data entry into standardized electronic databases
Experience with data entry into drug safety databases such as ARISg/ARGUS, preferred
Associated topics: authorization, cbo, clerk, coder, coding, data, medical coder, medicare, receivable, review

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