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