Manager, Global Submission Management

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...