Manager, PV Ops

• Responsible for capturing and assessing single adverse event reports associated with client products on the client’s Drug Safety database, in accordance with client and applicable regulatory requirements

• Performing clear and accurate data capture/entry of case including book-in, completion of data entry of all fields on the basis of information provided in source documents, case assessment, coding of patient history, concomitant medications, event and drug terms using embedded dictionaries using Argus & & writing narratives

• Performing self QC of the case

• Ensuring MedRDA coding in accordance with “MedRDA Term Selection: points to consider” where applicable

QualificationsWe are looking for candidates with Science/Medicine degree: Minimum Qualification would be a University Degree in Pharmacy or a degree in Dentistry