Job Day to Day Responsibilities:
This role is responsible for managing non-clinical regulatory documents from draft through submission readiness. Key responsibilities include:

+ Receiving non-clinical reports from scientists and authors.

+ Performing an initial QC review of Word documents against sources to verify accuracy, formatting to Company Style Guide, and alignment with the StartingPoint Template

+ Conducting document formatting and ensuring compliance with company style guides.

+ Converting text, figures, and data into the appropriate formats, including text-to-table formatting and section-by-section document review.

+ Verifying accuracy between narrative content, tables, and figures.

+ Performing copyediting and document standardization.

+ Preparing documents for progression through the regulatory submission workflow.

+ Perform the full QC review on as many of the documents that are submitted t...