Job Information
Bristol Myers Squibb Director, Clinical Demand & Operations Planning (CD&OP) Execution Lead in Moreton, United Kingdom
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 .
Week are seeking a Director, Clinical Demand & Operations Planning (CD&OP) Execution Lead. This individual will:
Lead the coordination, execution, and continuous improvement of Demand Alignment (DAM), Supply Review (SRM), and Clinical D&OP (CD&OP) forums, including agenda development, timing plus scheduling, material preparation, and effective escalation.
Post meetings ensure follow through on decisions, actions, and risks. Contributes to Executive S&OP discussions as appropriate.
Serve as the CD&OP Execution Lead, ensuring disciplined execution and documentation of supply and/or demand gaps, risks, resolutions, and recommendations for escalation to Executive S&OP.
Partner with Clinical Operations and cross functional R&D stakeholders to bridge supply chain expertise with market and study knowledge, enabling resolution of business-critical issues and informing key strategic decisions within Clinical Supply Chain.
Partner with S&OP peers in Pharm/Bio and Cell Therapy and BP&T to drive a continuous improvement mindset, as appropriate identifying suitable digital tools to enhance overall CP&OP processes.
Key Responsibilities:
Execute and sustain an integrated CD&OP operating cadence, ensuring a seamless flow of information, decisions, and escalations across Demand Alignment, Supply Review, Finance, Therapeutic level CD&OP, CSC level CD&OP, and Executive S&OP forums.
Coordinate and execute CD&OP related meetings, including development of required reports and metrics, documentation of Clinical Supply Chain gaps plus resolutions, and preparation of agendas and recommendations for Executive level review.
Support and contribute to Executive S&OP by managing timing plus scheduling, driving coordination of high-quality materials, and ensuring key risks, tradeoffs, and decisions are communicated clearly; enabling proactive plus timely decision making.
Partner with Demand and Supply Planning to ensure overall plan quality by driving S&OP best practices, improving forecast accuracy, and strengthening performance metrics, including financial measures.
Ensure supply risks, issues, and resolutions are appropriately escalated and cascaded through defined governance pathways to enable proactive, efficient risk management.
Participate in GPS and R&D Finance and/or Comparator Reviews to support adherence to approved budget plans and financial assumptions.
In collaboration with TA pillars, validate the quality of patient enrollment forecasts provided to Clinical Supply Chain and assess potential impacts to supply and demand risk.
Partners with the GDO and Finance to operationalize the CD&OP process attending the Demand Alignment meetings and running the Supply Review meetings from the products that they have responsibility for. Identifying opportunities or issues that need to be escalated potentially as high as the Executive S&OP meeting.
Identify gaps and inefficiencies within the CD&OP process and lead continuous improvement initiatives aligned with business priorities.
Provide training and coaching to stakeholders, establishing clear expectations for roles, responsibilities, and accountabilities within the CD&OP process.
Collaborate with Clinical Supply Chain Business Unit Heads and governance forums to align-on business priorities, performance, and key challenges.
Qualifications & Experience:
BA/BS degree in Supply Chain, Engineering, Business, or a related technical discipline required; advanced degree (Masters or MBA) preferred.
Deep understanding of how demand forecasts translate into operational and financial planning, performance measurement, and executive decision-making.
10+ years of experience leading end-to-end clinical supply chain planning processes-including demand forecasting, supply and inventory planning, and S&OP type execution-within a global, matrixed organization.
Leadership in global process implementation and governance (i.e. S&OP), with demonstrated ability to improve decision quality, speed to action, and enterprise alignment.
Strong project management and change leadership capabilities, with experience driving transformation in complex, fast-paced environments.
Exceptional interpersonal, collaboration, and cross-functional negotiation skills, with a demonstrated ability to influence, align, and gain commitment from senior stakeholders.
Highly effective communicator with outstanding executive-level presentation and business case development skills, capable of delivering clear, concise messaging to various leaders within the organization.
Demonstrated ability to resolve conflict, evaluate trade-offs, and make sound decisions under time pressure.
Proven people leader with experience building, developing, and retaining high-performing teams, fostering a culture of empowerment, accountability, innovation, and inclusion.
Results-oriented leader with the ability to execute strategy, manage competing priorities with agility, and consistently meet critical milestones and deadlines.
Strong stakeholder management skills, with a track record of developing, communicating and securing alignment on execution.
#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:
Madison - Giralda - NJ - US: $193,150 - $234,057
Princeton - NJ - US: $193,150 - $234,057
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 rate 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. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include:
Paid Time Off
US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
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/ (https://careers.bms.com/eeo-accessibility) 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.
R1601381 : Director, Clinical Demand & Operations Planning (CD&OP) Execution Lead Company: Bristol-Myers Squibb
Req Number: R1601381
Updated: 2026-04-16 03:56:17.849 UTC
Location: Uxbridge-GB
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.