Location
Wilmington, DE, United States
Posted
July 10, 2026
Job Description
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...
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...