Senior Manager, Program Management

Bristol-Myers Squibb Co; Warszawa; On-site; PLN 222,000 - 269,000; Full time

Job summary

Bristol-Myers Squibb Co. in Warsaw, Poland, seeks a Senior Manager, Program Management to lead cross-functional planning, oversee execution, and drive governance with minimal supervision. You will manage project plans, budgets, risk mitigation, and resource forecasting within a matrix environment.

The role emphasizes independence, leadership of PM sub-teams, and collaboration with Clinical, Regulatory, and Safety partners to ensure timely development milestones and robust governance.

Qualifications

• BS/MS degree in a scientific discipline with 5 years of drug development experience and 3 years in DD PM.
• PMP certification preferred.
• Experience with drug development processes from IND/CTA to marketing authorization.

Responsibilities

• Maintain project plans in the ePlan enterprise tool for each assigned project.
• Manage budget and resource health for each project.
• Lead or support risk management processes and mitigation planning.
• Ensure cross-functional alignment across Clinical, Regulatory, CMC, Safety, and others.

Skills

Project management

Leadership

Communication

Risk management

AI tools

Time management

Education

BS/MS degree in a scientific discipline

PMP certification

Tools

Planisware

Microsoft Project

Microsoft Planner

Job description

Position Summary

The Senior Manager, Program Management role serves as an experienced PM who operates with meaningful independence under the matrix leadership and supervision of a Program Management Lead (or GPT PM). They are assigned at the project level (asset indication) and/or sub-team level to deliver integrated cross-functional planning, oversee execution and administrate the PM sub-team(s) independently or in partnership with a more senior PM with minimal day-to-day supervision.

Duties/Responsibilities

They maintain project plans in the ePlan enterprise tool for each assigned project. Management of ePlan projects includes and is not limited to:

• Maintaining the latest development strategy
• Ensuring all metadata is accurate and up to date.
• Generating project level scenario plans.
• Managing resource forecast drivers.
• Creation of high-level timelines via approved tools and standards.
• Maintaining ePlan data quality at or above defined standards.
• Maintain a separate detailed project plan and timelines in Microsoft Project or Planner (system selection and standards pending) for the current stage of development or upcoming stage of development.
• Ensuring clear visibility and management of the networked critical path.
• Timing from this plan should inform updates to ePlan.
• Administrates the PM sub-team individually or in partnership with a more senior PM.
• Participates in GPT sub-team meetings as the direction of the Program Management Lead ensuring strategic alignment and rigorous execution per governance approved timing and budget.
• Leads or partners with a more senior PM to deliver risk management processes.
• Develops and monitors mitigation plans for high probability high impact risks.
• Supports the Program Management Lead in preparation for governance including generation of development timelines, alternative scenarios, budget and resource requirements.
• Oversee the budget and resource health for each assigned project and elevate any issues / concerns.
• Serve as a delegate or deputy for the GPT Program Management Lead if requested.
• Drives cross-functional alignment across functional partners (Clinical, Regulatory, CMC, Safety, and others)
• Change agent for continuous improvement and transformational initiatives within the PM function.

Reporting Relationship:

Reports into a PM Portfolio Lead (Group Lead) or Director, Program Management.

Qualifications

• BS/MS degree in a scientific discipline in combination with 5 years of drug development experience and 3 years in DD PM is required.
• PMP® certification is preferred.
• Solid experience and understanding for drug development processes ranging from IND/CTA submission to submission for marketing authorization.
• Demonstrated leadership soft skills, able to speak up within a team of subject matter experts and influence without authority.
• Experience and strong aptitude for commonly used project management tools including but not limited to Planisware, Microsoft project, or Microsoft Planner.
• Able to prepare meeting agendas and succinctly summarize meeting outcomes and project details leveraging AI tools.
• Proficient in core project planning and control methods and is able to independently construct and communicate critical path and development scenarios.
• Familiarity with standard PM Risk Management practices and methodologies.
• Able to drive execution while monitoring time, resource and budget.

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: zł222,360 - zł269,448 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 [e-mail]. 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 [e-mail] 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.

R1606668 : Senior Manager, Program Management Data Privacy Link

We’re creating innovative 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.