Posted:18 hours ago|
Platform:
Work from Office
Full Time
This role is responsible for creating and validating ad hoc reports and queries needed to support Pharmacovigilance and signal detection activities as well and the review of these reports and queries to verify that they are accurate and consistent with the request from the subject matter expert This role encompasses many of the operational aspects within the System Support and Data Management unit. This role works directly with all GPV stakeholders, including GSOs, PV Scientists, to accurately interpret and translate business needs into the appropriate technical language to ensure that configuration, operations, validation, and/or analytic reporting deliverables meet business needs. This role is responsible for the oversight and management of various aspects of the safety database system as well as direct involvement and oversight of projects designed to deliver enhancements, change controls and future tools to support GPE. Additionally, the role will have oversight for multiple vendor activities supporting the SSDM team. The incumbent works with all Safety System and Data Management stakeholders to ensure accurate planning and execution of critical database system activities The role can also participate in the configuration of the safety database as well as the development, validation and maintenance of the system enhancements including the generation and approval of documentation to support the customer methodology PUMA (Project Unified Methodology Approach). It is important that the role has a strong PV knowledge and working relationships with the user community as well as the Information Technology (ITS) department.
Iqvia Biotech
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