Job Description

This team ensures Pfizer's Clinical Study Report (CSR) management meets global agency standards and manages regulatory reporting, dossier development, and submission activities for Global Regulatory & International Operations (RIO). Members in the team oversee and manage end-to-end lifecycle development of CSR to support Pfizer's global drug registration and approval processes, including submission, publishing, and archiving of related reports and documents.

Associate

  • Lead the coordination, compilation, quality control, approval and post-approval processes associated with development of Pfizer global CSRs
  • Create CSR mockups in System and populate document templates
  • Project manage CSR compilation, approval and publishing activities
  • Execute submission ready Quality Control (QC) on CSR components and structure
  • Communicate with function lines regarding issues with CSR components and seek resolutions
  • Seek approval from signa...

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