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Bristol-Myers Squibb is hiring a Manager, Global Submission Management

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Job Description

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Shape How Medicines Reach Patients Worldwide 

What if your work didn’t just support submissions… but helped accelerate how innovative therapies reach patients across the globe? 

At Bristol Myers Squibb, we’re transforming how regulatory submissions are delivered, making them faster, smarter, and globally aligned. 

 

Your Mission 

Own and drive the delivery of IND and global regulatory submissions, ensuring high-quality, compliant dossiers reach health authorities on time, while helping teams operate as one connected global system. 

 

What Your Week Might Look Like 

  • Leading cross-functional discussions to align submission strategy and timelines 

  • Coordinating IND or marketing application deliverables across global teams 

  • Managing eCTD submissions from planning through to delivery 

  • Tracking progress, identifying risks, and keeping critical milestones on track 

  • Working in Veeva RIM and the Lorenz docuBridge publishing tool to manage and monitor submissions 

 

What You’ll Do 

  • Drive end-to-end regulatory submissions (IND + global applications) 

  • Collaborate with global stakeholders to deliver high-quality, compliant dossiers 

  • Manage timelines, risks, and dependencies across complex submissions 

  • Execute and oversee eCTD publishing activities 

  • Contribute to process improvements and innovation initiatives 

 

You’ll Thrive If You 

  • Take ownership and enjoy driving complex workstreams 

  • Like balancing strategy with execution 

  • Are comfortable working in fast-paced, global environments 

  • Enjoy solving problems and improving how things are done 

 

Your Background 

  • Bachelor’s degree (science or related field preferred) 

  • 3+ years in regulatory submissions 

  • Experience with IND, eCTD, or global submissions 

  • Familiar with Veeva RIM or Lorenz docuBridge 

  • Strong communication and project management skills 

 

Why This Role is Different 

  • Real exposure to global submissions and health authorities 

  • Opportunity to work across multiple regions and projects 

  • High visibility within regulatory and cross-functional teams 

  • A chance to improve how submissions are developed and delivered across a global network, helping innovative medicines reach patients faster 

Flexibility 

Hybrid work with up to 50% work from home. 

Apply 

Ready to step up? Apply now and help shape the future of clinical trial submissions. Please submit your CV in English. 

#LI-Hybrid 

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:

Warsaw - PL: zł174,980 - zł212,026

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.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

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 adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

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

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 you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1601844 : Manager, Global Submission Management
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Salary Information

Salary: $75000-110000

🤖 This salary estimate is calculated by AI based on the job title, location, company, and market data. Use this as a guide for salary expectations or negotiations. The actual salary may vary based on your experience, qualifications, and company policies.

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