Associate Director, Procurement, Clinical Development

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.

Bristol Myers Squibb (BMS) is seeking an accomplished procurement professional to advance category excellence within Specialized Services, across categories such as Regulatory and Patient Safety. This Associate Director will operationalize the Clinical Development Procurement (CDP) transformation agenda within these specialized areas—enhancing supplier partnerships, compliance rigor, and delivery performance through data-driven sourcing, analytics, and agile governance frameworks. This role will translate enterprise procurement frameworks into category strategies that enable operations across Regulatory and Patient Safety categories.

The role requires strong business acumen and the ability to influence across functions, ensuring that enterprise procurement practices are effectively adopted and optimized through technology, analytics, and supplier partnerships. This position partners closely with the stakeholders within the Clinical Development functions as well as Category Managers across R&D Procurement to ensure cross-domain alignment on supplier innovation, digital transformation, and operational excellence .

Major Responsibilities and Accountabilities:

Category Management & Procurement Excellence

• Responsible for procurement activities—including identification, assessments evaluation of suppliers with demonstrated service excellence in assigned categories. As applicable review, drafting, negotiation, and redlining supplier proposals—across novel or technically complex categories with limited legal supervision.

• Lead sourcing events to deliver integrated sourcing strategies and ensure successful program execution.

• Implement data-driven category strategies that deliver measurable value, productivity gains and service excellence.

• Serve as an accountable point of contact for internal Clinical Development stakeholders, external industry partners, and strategic suppliers, ensuring alignment between business needs and category strategies.

• Prepare and present strategic recommendations, insights and progress updates to senior leadership to support informed decision-making.

Supplier Performance and Risk Management

• Partner with SRM teams to support supplier segmentation and formalize Supplier Relationship Management (SRM) programs for key strategic partners.

• Drive value-creation targets with business stakeholders and ensure regular performance reviews with measurable outcomes across respective categories.

• Ensure that contractual arrangements embed KPI-driven accountability and compliance obligations.

• Proactively identify, assess, and mitigate supplier and supply-chain risks, ensuring resilience and continual focus on quality deliverables.

Cost Management and Value Optimization

• Deliver cost-reduction, value-enhancement, and productivity initiatives across assigned R&D categories.

• Support, monitor, and forecast budgets, ensuring adherence to financial targets and alignment with enterprise investment priorities.

• Lead negotiations and strategic deal structuring to secure optimal commercial terms, value delivery, and risk balance across supplier portfolios .

Governance, Compliance & Reporting

• As relates to the categories in scope, support governance structures that drive disciplined decision-making, transparency, and compliance with corporate and regulatory standards.

• Monitor adherence to contractual, financial, and ethical requirements, partnering closely with Legal, Privacy, and Compliance.

• Provide regular reporting and performance insights into leadership, highlighting progress, risks, and mitigation actions.

Innovation and Continuous Improvement

• As relevant to the categories in scope, build and maintain strong partnerships with R&D, Clinical Development, Finance, Legal, and other functional leaders to ensure cohesive strategy execution.

• Support adoption of advanced procurement practices, automation, and emerging digital technologies.

• Stay abreast of industry trends and market evolution to ensure BMS maintains a leadership position in R&D procurement excellence.

• Foster external partnerships with suppliers and industry consortia to benchmark best practices and identify collaboration opportunities.

• Provide informal coaching or mentoring to junior procurement team members as needed.

Qualifications

Minimum Requirements

• Minimum education of a B.S./B.A. is required; M.S./M.B.A. is preferred.

• Minimum of seven (7) years of relevant experience in biopharmaceuticals, life sciences, or related industry with at least five (5) years of experience in a strategic procurement, category management or a comparable function is required.

• Demonstrated experience leading sourcing initiatives, supplier negotiations and cross-functional collaboration.

• Strong knowledge of category management and advanced strategic sourcing methodologies.

• Experience supporting cost reduction, value improvement programs or productivity initiatives.

• Exposure to global or cross-functional teams preferred.

• Travel: Travel may be required (domestic and international) for business meetings, supplier visits, and cross-functional engagements as needed.

#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:

Tampa - FL - US: $161,250 - $195,391

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

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 View email address on us.fitly.work. 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:

Data Protection

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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 View email address on us.fitly.work. 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.

R1605582 : Associate Director, Procurement, Clinical Development