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.

Shape How Medicines Reach Patients Worldwide

The Opportunity

What if your workdidn’tjust support submissions… but helped accelerate how innovative therapies reach patients across the globe?

At Bristol Myers Squibb,we’retransforming how regulatory submissions are delivered—making them faster, smarter, and globally aligned. As aSenior Specialist,you’llplay a critical role in driving high-quality submissions and improving how teamsoperatetogether globally.

Your Mission

Own and deliver IND and global regulatory submissions end-to-end, ensuring compliant, high-quality dossiers reach health authorities on time—while driving consistency, efficiency, and operational excellence across submission activities.

What Your Week Might Look Like

Leading coordination of submission activities across global teams

Partnering with stakeholders to define submission strategy and timelines

Managing IND and marketing application submissions from planning through to delivery

Tracking progress,identifyingrisks, and ensuring milestones stay on track

Executing eCTD publishing and managing submissions via HA portals

Working in Veeva RIM andLorenzdocubridgepublishing tool tomonitor, report, and manage content

WhatYou’llDo

Drive end-to-end submission management (IND and global applications)

Collaborate with cross-functional and global stakeholders to deliver compliant dossiers

Manage timelines, risks, and dependencies across submission projects

Execute and oversee eCTD publishing activities

Maintain submission data, reporting, and tracking in Veeva RIM

Coordinate non-eCTD submissions with international teams

Ensure consistency across submissions, studies, and regions

Contribute to continuous improvement and innovation initiatives

You’llThrive If You

Take ownership and proactively drive deliverables

Enjoy balancing coordination, execution, and problem-solving

Are confident working across global, matrixed environments

Have strong attention to detail and organisational skills

Are motivated to improve processes and embrace digital tools and automation

Your Background

Bachelor’s degree (science or related field preferred)

Experience in regulatory submissions (typically 1–3+ years)

Understanding of global regulatory requirements and submission processes

Exposure to IND, eCTD, or global submissions

Familiarity with tools such as Veeva RIM andLorenzedocuBridgepublishingtoolis a plus

Strong communicationand stakeholder engagement skills

Ability to manage priorities and deliver against timelines

Why This Role is Different

Meaningful exposure to global regulatory submissions and health authorities

Opportunity to work across multiple regions and therapeutic areas

Strong visibility within regulatory and cross-functional teams

A chance to improve how submissions are delivered—at scale and with impact

Flexibility

Hybrid role with the option to work remotely up to50% of the time, aligned with business and collaboration needs.

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: zł116,650 - zł141,347

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 adastaffingsupport@bms.com. 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 TAEnablement@bms.com 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.

R1601389 : Senior Specialist, Submission Management

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We’re creatinginnovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.

Senior Specialist, Submission Management

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