Role - Veeva Regulatory Information Management Database (RIM)
6+ months contract
Location - South San Francisco, CA
Start: ASAP
Responsibilities include:
• Create standard operating process for Veeva naming conventions (Metadata) for regulatory documents.
• Create, assign, and manage Veeva workflows for regulatory documents as needed.
• Regulatory Operations trainer for Veeva-RIM
• Transfer current Module 3 Regulatory Documents from SharePoint into Veeva system.
• Assist with archiving documents from Health Authorities and Regulatory Staff into Veeva (RIM)
• Technical editing/formatting of documents for Regulatory Submissions (Starting Point template documents)