- Clinical research jobs
- Sr. Prod Data Input Associate
Sr. Prod Data Input Associate
IQVIA Holdings Inc.
Pasig City, Philippines
Role Purpose:
Under guidance maintains more complex reference files needed by IQVIA production.
Principal Accountabilities:
- Perform maintenance of reference data (Product) as required for AU/NZ Production.
- Performs research (e.g. internet search, source books, manufacturer websites etc.) to gather information from third parties that will augment the completeness or accuracy of IQVIA reference data.
- Follows standard practices and procedures in analysing situations or data from which answers can be readily obtained.
- Solicits 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.
- Receives input to the reference process from other IQVIA production processes.
- Validates that the information gathered from third-party sources represents accurate new data that should result in a change, addition, or deletion in IQVIA’s existing reference data.
- Identifies required changes to the existing reference file.
- Updates IQVIA reference file(s) and databases.
- Produces files and outputs for specified production and quality control processes, client support activities, etc.
- Responds to queries on reference data (as required).
Minimum Education, Experience, & Specialized Knowledge Required:
- Bachelor’s degree or equivalent in Pharmacy, Nursing, or related fields
- Preferably at least 1-year experience with Production and with clear understanding of the different processes and dynamics within the group.
- Previous experience in any medical account would be an advantage
- Strong interpersonal and written and verbal communication skills.
- Strong customer focus, an attention to detail and excellent analytical and problem-solving skills
- Ability to proactively identify complex problems and needs and develop solutions/recommendations to solve problems.
- Ability to work under time constraints and changing work volumes
- Strong PC literacy skills including Word, Excel and Access, with an understanding of relational databases
Additional Requirements:
- The job requires flexibility to transition to a new project will require quick grasp on different processes from time to time.
- Specialized knowledge of an area of the company's products, pharmaceutical industry or field specific to a major function
Job posted: 2023-11-16