Labcorp Medical Writing Publisher - I in Helana, Montana
Medical Writing Publisher I
Office based in Madison, WI or US Remote based
The Medical Writing Publisher I compiles an electronic version of the final regulatory documents and creates the associated PDF files. Performs bookmarking and hyperlinking of the final PDF of the regulatory documents prior to client receipt. Compiles informational clinical study report appendices and inserts clinical study report tables, figures, and listings into appropriate sections. Reviews timelines and informs Medical Writer, Project Manager, and/or Client of current status. Assists with document formatting.
Publishes Labcorp Drug Development's standard documents and some client-specific projects.
Performs peer review QC for published and compiled documents.
Ensures documents are in compliance with the relevant regulatory guidelines.
Understands the task to be completed and the budgeted hours. Monitors the actual hours and escalates to a Manager if these hours will exceed the budgeted hours.
Collaborates with writers to discuss discrepancies, omissions, and errors.
Participates in staff meetings and project team update meetings as appropriate.
Completes reviews within given timelines.
Performs any other duties as assigned by Manager or Supervisor.
Associate degree or Bachelor of Science/Arts (BS/BA) degree.
Minimum 0 to 2 + years of experience.
Additional experience may be substituted for education requirements.
Ability to efficiently use basic software (eg, Adobe Acrobat, Word, Excel, PowerPoint).
Knowledge and understanding of publishing tools.