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 rich in diversity. 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.

Global Clinical Supply Chain (CSC) is a new organization within Global Supply Chain (GSC).  GSC’s vision is to be a patient-centric, integrated supply chain, launching and supplying innovative products that deliver hope to patients through life-changing medicines.  The Global Clinical Supply Chain (CSC) organization contributes to this vision by working seamlessly across the enterprise to supply BMS’s global portfolio of clinical studies.  CSC represents an innovative organizational model, an innovation that enables BMS for a future in which commercial supply chains will be increasingly similar to clinical supply chains due to advances in personalized medicine and targeted therapies.  

Position Summary   

This position is responsible for all matters pertaining to the global forecasting and planning of investigational materials for clinical studies with a primary responsibility for leading the development and execution of investigational material supply strategies for global studies. The incumbent will lead a group of Trial Supply Managers and/or Inventory Planning & Coordination Specialist/Managers responsible for obtaining long term forecasts and developing supply strategies for each study. Working as a key member within Trial Supply Management, the position will proactively recognize and address any technical and regulatory issues associated with the product’s quality or suitability for intended use. The incumbent will also be considered a subject matter expert on all information regarding the global use of investigational material in clinical studies. 

Roles and Responsibilities 

• Directly oversee and manage the development and implementation of supply strategies for all investigational material based on study needs and scientific and regulatory confines of the drug development. 

• Directly oversee the management of investigational material inventories, related study forecasts and assessments. 

• Accountable for timely, cost effective and high-quality execution of approved strategies. 

• Manage project budget and project timelines, with the support of the Clinical Supply Program Team, Global Clinical Supply Chain management and functional leadership, ensuring appropriate and timely resource allocation to achieve project goals and deadlines. 

• Provide to functional head, and continuously update, a balanced appraisal of the project status, including risk, cost, and value to stakeholders. 

• Provide direction to Trial Supply Managers on study protocols for packaging and label design, distribution plan and IRT design for global studies. 

• Provide leadership and vision needed to create, implement, execute and maintain processes that ensure production deliverables and cost effectiveness. Influence and counsel senior management in the establishment of these systems. 

• Identify and evaluate fundamental issues pertaining to the clinical supply chain through assessment of intangible variables and provide plans for resolution. 

• Independently make decisions to ensure effective utilization of global investigational material resources based on capacities and resources. 

• Communicate project status and readiness, business and technical issues and risks and options across function lines and management up to and including executive levels. 

• Participate in and provide leadership to Trial Supply Management process improvement Initiatives resulting in cohesive supply chain activities 

• Foster strong collaboration with all functional partners, including but not limited to Global Drug Development, Pharmaceutical Development, Product Development Quality (PDQ), External Vendors and Medical, to assure clinical trials are conducted efficiently and effectively solve abstract problems across functional areas of the business. 

• Manage a team of Trial Supply Managers and/or Inventory Planning & Coordination Specialist/Managers. 

• Hire, train and retain team members to develop the second line of management. 

• Performs other tasks as assigned. 

Skills and Qualifications 

• 10+ yrs. experience in the pharmaceutical industry with 7+ yrs. experience in drug development, clinical supply chain management and/or clinical manufacturing and 3+ years in project management OR Equivalent experience. 

• An equivalent combination of education and experience may substitute. 

• Experience across multiple functional areas (i.e. clinical, regulatory, quality) demonstrating a broad understanding of pharmaceutical development. 

• In-depth knowledge of all phases of drug development, of the functions and processes relevant to drug development, and project management principles applicable to the biopharmaceutical environment. 

• Extensive experience with planning and execution of investigational materials supply strategies. 

• Demonstrated strategic and leadership skills. 

• Proven ability to effectively develop, communicate, and gain support for execution plans with a wide range of stakeholders. 

• Result oriented individual to execute strategy and meet objectives.  

• Experience managing change in a dynamic, complex environment. 

• Strong background in cGxPs and ICH requirements. 

#LI-Remote

The starting compensation for this job is a range from $156,000 - $195,000

plus incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills and the geographic location where work is performed. Final, individual compensation is decided commensurate with demonstrated experience. For more on benefits, please visit our BMS Careers Site. Eligibility for specific benefits listed therein may vary based on job and location.

Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.

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.

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 an inclusive culture, promoting diversity 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 a diverse 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.

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 [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.