Bristol Myers Squibb is seeking a Senior Documentation Specialist to independently manage eDMS processes, publish regulatory documents, and collaborate with GSRD and external authors. The role involves mentoring, ensuring submission-ready formatting, and coordinating protocol and CSR documents across teams.
With a BS/BA and 2-4 years in regulatory documentation, you will use Acrobat/ISI toolbox and a document management system to uphold eCTD standards while driving timelines and quality.