Bristol Myers Squibb
Pharmaceutical
Director,GlobalScientificandRegulatoryDocumentation,ContentStrategy
“Director, Global Scientific and Regulatory Documentation, Content Strategy at Bristol Myers Squibb. Skills: Regulatory documentation, Content strategy, GenAI, Team leadership. Optimize content and documentation delivery. Assess resource requirements for projects”
What You'll Achieve.
Support BMS pipeline; Support quality and content flow; Support departmental metrics and analytics; Achieve superior business performance
Industry & Context.
What They're Looking For.
Must Have
10 years in pharmaceutical regulatory documentation, PharmD/PhD/MD in relevant scientific discipline, Master's/Bachelor's degree with 10 years experience, Proven record managing group/project team, Significant experience writing high-quality regulatory documentation, Experience managing project teams and process workflows, Experience working in rapidly changing environment, Experience mentoring and professional development, Advanced understanding of global pharmaceutical drug development, Demonstrated ability to manage timelines and quality, Experience in state of the art documentation processes and technology
Nice to Have
Prior regulatory documentation leadership, Development and approval of new drug applications/dossiers
What You'll Do.
Optimize content and documentation delivery
Assess resource requirements for projects
Assign resources according to priorities
Prepare criteria for external documentation support
Review regulatory documentation
Review clinical documentation
Review safety documentation
Recruit scientific writers
Train scientific writers
Set clear performance standards
Provide feedback and coaching
Identify training needs
Hold group members accountable
Provide performance evaluation input
Support skillset development
Lead innovation projects
Contribute to innovation projects
Automate regulatory writing processes
Optimize regulatory writing processes
Serve as GenAI champion
Support authoring workflows evolution
Support standardization
Support efficiency across documents
Ensure regular entry of metadata
Influence other functions
Develop training on regulatory documents
Provide training to writers
Develop resources for writing team
Facilitate proactive sharing of knowledge
Facilitate key learnings sharing
Interface across multiple functions
Mediate conflict resolution
Champion organizational culture
Promote behaviors for synergies
Promote behaviors for business performance
How You'll Work.
Team & Collaboration
Cross-functional collaboration; Cross-functional communication; Cross-functional team
Communication Scope
Cross-functional communication
Process & Methodology
Process workflows
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