Drug Safety Associate Opportunity Available in Delaware

Smith Hanley is seeking an experience Drug Safety Associate for a local pharmaceutical company in the Delaware area. The successful candidate will be responsible for: -Data entry of nonserious and serious adverse event case reports including coding. Interpretation of data, coding of disease terms, drugs, events. -Perform triage and processing of large volumes of medical records. -Perform all activities to ensure that global and local regulatory timelines are met. Requirements:RN/Pharm D. Individual must have Drug Safety experience in case processing, medDRA coding. Must be able to data enter initial and follow-up adverse events into drug safety database, including interpretation of medical information. Must have good coding and writing skills to ensure consistency with case entry. Prior nursing or pharmaceutical experience preferred. Good analytical, organizational and computer skills a must.  If you are interested in applying for this exciting career opportunity, please email your resume to Lynn at lrodriguez@smithhanley.com . If you would like to be considered for this opportunity, please forward your resume to the email address provided below. If you meet the minimum requirements someone will be in touch with you to discuss the specific details.