Bristol Myers Squibb

Bristol Myers Squibb

Posted via Workday

Senior Specialist, Document Management

Apply by Nov 14, 2026

Posted Sep 3, 2026

Role at a glance

Job function
Legal & Compliance Compliance & Regulatory Affairs
Salary
Not Disclosed
Location
Warsaw-WeWork-PL
Work arrangement
Hybrid
Employment
Full-time
Experience
Senior Level Minimum of BS/BA degree with approximately 2-4 years of regulatory documentation experience in document management repositories, submission readiness formatting and publishing work flows.
Education
Minimum of BS/BA degree

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Role Summary

AI-generated

The Senior Specialist independently manages eDMS processes, submission-readiness formatting, and publishing for regulatory documents, including protocols and clinical submission documents. The role also coordinates document inputs and works with internal partners and external authors to meet submission requirements.

What You'll Do

  • Manage eDMS processes and publish protocol and submission documents in partnership with internal teams and external authors.
  • Provide training, mentoring, and troubleshooting assistance on eDMS, templates, formatting, and publishing workflows.
  • Define submission-readiness requirements and manage remediation, eDMS import, and publishing of externally authored PDFs.
  • Coordinate collection and review of ICH non-data-driven appendices for clinical study reports.
  • Coordinate, compile, or author selected protocol and submission document types, integrating scientific and regulatory input.
  • Contribute to model document updates and process-improvement workstreams, including automated and digital solutions.

Generated from the employer's posting. Verify important details before applying.

View full posting

Qualifications

Requires a BS/BA degree and approximately 2–4 years of regulatory documentation experience in document management repositories, submission-readiness formatting, and publishing workflows. Requires knowledge of desktop applications, Word template macros, model documents, eCTD-compliant document creation and remediation using Acrobat and ISI toolbox, document management systems, publishing processes, and troubleshooting. Strong organizational, communication, facilitation, and interpersonal skills are required to manage timelines and quality and work in a matrix team environment.

Original job description

Content provided by the employer

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.


The Senior Specialist, Documentation - based in Warsaw - independently manage eDMS processes within scope, submission-readiness formatting, and publishing of regulatory documents including clinical study reports, Investigator Brochures, safety aggregate reports, module 2 summaries and clinical protocol documents.

Duties/Responsibilities:

  • Independently partner with GSRD and external authors for management of eDMS processes within scope and document publishing of protocol and submission documents.

  • Mentor, train and provide troubleshooting assistance to GSRD personnel and external authors in the eDMS, Core Template, submission readiness formatting and publishing work processes.

  • Collaborate with cross-function business partners providing direction in SRC formatting and publishing of protocol and submission related documents

  • Lead cross functional business partners in defining submission-ready requirements for externally authored regulatory documents.  Independently manage submission readiness remediation, eDMS import and publishing of externally authored PDF files. 

  • Independently manage collection and review of ICH non-data driven appendices for CSRs. Direct cross functional business partners (CTAs, Protocol Managers) in defining submission-ready requirements for ICH non-data driven appendices. 

  • Contribute to GSRD model document updates and system approval processes.

  • Independently coordinate, compile and/or author select protocol and submission documents types ensuring integration of scientific and regulatory input from team members.

  • Participate in continuous improvement workstreams to enhance quality and increase efficiency of document processes, including automated and digital solutions for development of regulatory documentation.

Qualifications

  • Minimum of BS/BA degree with approximately 2-4 years of regulatory documentation experience in document management repositories, submission readiness formatting and publishing work flows.

  • In-depth understanding of desktop applications, word template macros, model documents and submission readiness formatting for creation of eCTD compliant regulatory documents.

  • In-depth understanding of Acrobat and ISI toolbox usage in creation and remediation of eCTD compliant regulatory documents.

  • In-depth understanding of a document management system for assembly and management of regulatory documents.

  • Understanding of document publishing processes across document types

  • Demonstrated troubleshooting skills in eDMS, submission readiness formatting and document publishing work flows.

  • Ability to manage timelines and quality of work using strong organizational, communication, facilitation, and interpersonal skills

  • Effective interpersonal skills to work well in a matrix team environment and with colleagues at all levels in the organization

Please note that this position is not a remote working opportunity and is based in the local BMS office, following a hybrid work model with at least 50% onsite attendance at your assigned facility.

#LI-Hybrid

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:

Warsaw - PL: zł144,100 - zł174,616

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.


How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.


Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.


Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.


For roles based in Los Angeles County only:  If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/


Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.


Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.


If this posting is missing required information required by local law or incorrect, contact BMS at [email protected] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.



R1601850 : Senior Specialist, Document Management
Bristol Myers Squibb

About the company

Bristol Myers Squibb

Large Enterprise

Bristol Myers Squibb is a global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a focus on oncology, immunology, and cardiovascular health, the company leverages advanced science and technology to create transformative therapies that address critical unmet medical needs. Operating in more than 70 countries, Bristol Myers Squibb emphasizes collaborative efforts and strong partnerships in research and development to drive advancements in healthcare and improve patient outcomes worldwide.