<ul><li>&nbsp;Responsible for executing GRO RIM operations in line with Work Instructions and SOPs.</li><li>Primarily will be RIM Central Data Service related product registration data management (includes the procurement of data from source regulatory documentation which requires a thorough understanding of the structure and contents of a regulatory dossier, and a thorough understanding of the data structures applicable to registration data and the related system workflows).</li><li>Perform Quality Control (QC) and data integrity checking, as part of the RIM Central Data Services operation, to confirm the accuracy and completeness of the Teva Global Registration database.</li></ul>

Regulatory Information Management System (RIMS)