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Bristol Myers Squibb

Director, Clinical Supply Chain – Planning

Bristol Myers Squibb

. Manage domestic and international order fulfillment of clinical trial product, including Standard of Care products, for RayzeBio clinical programs .

Posted 10/6/2026full-timeRemote • United StatesLead💰 $190,989 - $231,434 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in managing clinical supply chain activities, including procurement, inventory management, and compliance with cGMP, GDP, and FDA regulations. Proven ability to lead and develop high-performing teams while optimizing supply chain processes and vendor relationships.

Highest-signal resume keywords
Supply Chain ManagementProcurement ManagementCGMP ComplianceVendor ManagementTeam Leadership

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Supply Chain OptimizationMaterial ManagementCost AnalysisContract NegotiationDemand PlanningS&OPInventory ManagementRegulatory ComplianceAnalytical SkillsStrategic Problem-Solving
Soft Skills
Excellent CommunicationStakeholder ManagementCollaborationEmpowermentInnovation
Tools & Technologies
Supply Chain Management MethodologiesProcurement Tools
Industry Keywords
BiotechPharmaClinical Trial ManagementLogisticsThird-Party Depot

About the role

Key responsibilities & impact
  • Manage domestic and international order fulfillment of clinical trial product, including Standard of Care products, for RayzeBio clinical programs
  • Manage clinical trial labeling, packaging, and distribution activities for externally manufactured products
  • Establish departments and teams responsible for Clinical Supply Chain, Planning, and Warehousing/Depot
  • Develop cost-effective material purchasing strategies aligned with organizational goals
  • Maintain supplier relationships and scout additional vendors
  • Oversee supplier identification and evaluation, contract co-negotiation, and agreement management
  • Serve as primary contact for corporate leadership and clinical stakeholders regarding clinical supply chain activities
  • Oversee relationships with external vendors, logistics providers, and third-party depots
  • Establish processes to monitor and manage inventory levels and prevent shortages or overstock
  • Conduct cost analyses, establish benchmarks, identify cost-saving opportunities, and optimize procurement strategies
  • Ensure compliance with cGMP, GDP, FDA, and other relevant regulatory requirements
  • Direct documentation, policies, and procedures for clinical supply chain activities
  • Oversee training, onboarding, and capability development for clinical supply chain teams
  • Build relationships with manufacturing, quality, regulatory, finance, and commercial teams
  • Evaluate spending operations and improve product quality and delivery timeliness
  • Develop and implement risk management procedures for shortages and supply chain disruptions
  • Attract, develop, supervise, and retain a high-performing procurement team
  • Foster empowerment, collaboration, innovation, and accountability
  • Ensure succession planning and professional development for key roles

Requirements

What you’ll need
  • Bachelor’s degree in Supply Chain Management, Engineering, Business, or related field
  • 10+ years of progressive experience in supply chain/procurement management within biotech, pharma, or comparable industries
  • Demonstrated experience in site operations, procurement, material management, and team leadership
  • Strong analytical, strategic, and problem-solving skills
  • Excellent communication and stakeholder management abilities
  • Deep understanding of cGMP, GDP, and FDA regulatory requirements
  • Experience with S&OP, demand planning, and supply chain optimization
  • Ability to work in a matrix environment and influence senior leaders
  • Proven experience developing and leading supply chain teams
  • Advanced proficiency in supply chain management methodologies and tools
  • Familiarity with vendor management, contract negotiation, and cost control processes
  • Willingness to travel up to 20% between Indianapolis, San Diego, and other relevant locations
  • Regular interaction within office, warehouse, and manufacturing environments, with PPE required in certain areas

Benefits

Comp & perks
  • Discretionary incentive cash
  • Stock opportunities
  • Wellbeing support
  • Retirement and financial protection benefits
  • Medical, dental, vision, life and disability insurance
  • Flexible Time Off (FTO) for U.S.-based exempt employees
  • 11 paid company holidays
  • 160 hours of paid vacation annually for new hires for non-exempt employees, RayzeBio employees, and employees located in Puerto Rico
  • 3 optional holidays for non-exempt employees, RayzeBio employees, and employees located in Puerto Rico
  • Paid sick leave, depending on eligibility
  • Up to two paid volunteer days per year
  • Summer hours flexibility
  • Leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs
  • Annual Global Shutdown between Christmas Day and New Year's Day
  • Reasonable workplace accommodations/adjustments and ongoing support for people with disabilities