Description
Under guidance, you will maintain reference files needed by IQVIA production.
Essential Functions You will perform research to gather information from third parties to augment the completeness or accuracy of IQVIA reference data. You will solicit information from other IQVIA departments to identify when and how to correct inaccurate data, delete data, or add new entries to make the reference files more complete. You will receive input to the reference process from other IQVIA production processes. You will validate that the information gathered from third-party sources represents accurate new data and recommend changes, additions, or deletions in IQVIA's existing reference data. You will identify required changes to the existing reference file. You will update IQVIA reference file(s) and databases. You will produce files and outputs for specified production and quality control processes, client support activities, etc. You will respond to queries on reference data, referring difficult queries to the team leader.
Qualifications
- High School Diploma or equivalent required
- Some work experience in a pharmaceutical environment required
- Good PC literacy skills, including Word and Excel
- Ability to carry out some analysis and information gathering to resolve problems on routine matters
- Developing knowledge of the company's products and pharmaceutical industry