Priyanka Kaveti

Etmf veeva vault immediate joiner 

Managing all centralized activities in support of global clinical trials and ensures clinical 
documentation in appropriate tools especially Veeva Vault.
 Responsible to classify the documents according to Country, Site or Trial Level 
depending on the status of the Site.
 Uploads documents into appropriate sections to ensure they are accurate and in 
compliant with ALOCA, ALOCA+ principles.
 All metadata mandatory fields are updated as per the instructions to retrieve them.
 Performs QC’s, if any quality issues encountered provides feedback on the same.
 Manages all study start up documentation activities for global clinical trials.
 Maintains and reviews Study SharePoint, and also does admin related works like 
giving access to certain documents for internal team.
 Acts as a primary contact for the entire study team from study start up to close out 
activities support of documents to eTMF for accuracy.
 Provides system support like eTMF-Veeva vault, Prism, etc.
 Maintains study timelines and resolves any issues on priority.
 TMF reconciliation work has been done on various projects.

M.Pharmacy  Pharma cuetics