Associate Director, Clinical Supply Lead (CSL)
Bristol Myers Squibb
9 hours ago
Remote friendly (Madison, NJ)
United States
Operations
Associate Director, Clinical Supply Lead (CSL)
Key Responsibilities:
- Execute strategic vision and direction for clinical asset planning; ensure alignment of asset/study plans with established strategy and recommend improvements.
- Oversee clinical supply planning for assigned assets/studies; support continuous improvement.
- Support and guide matrix team members within assigned assets/studies; strengthen clinical supply planning capabilities.
- Serve as the single point of accountability for clinical supply planning and execution for assigned assets/studies.
- Support CSC leadership preparing materials for governing bodies and key stakeholders; provide subject-matter expertise for asset-related decisions.
- Execute CSL processes; contribute to continuous improvement using asset/study-level KPIs and performance metrics.
- Resolve issues within asset/study scope and timely escalate higher-impact risks.
- Act as primary Clinical Supply Chain point of contact for assigned compounds and studies; lead global supply strategy communications as appropriate.
- Lead matrix teams to develop and implement integrated cross-functional strategies, resourcing, and plans to ensure continuous investigational product supply and timely delivery of quality clinical supplies.
- Oversee supply forecast development for complex studies; evaluate/refine clinical development plan and protocol analysis; monitor inventory/drug utilization vs forecast, considering country requirements and logistics.
- Partner with GDO and Finance to operationalize the CD&O P process (attend Demand Alignment meetings; run Supply Review meetings).
- Assist with adoption and sustainment of a data-enabled CSL ecosystem integrated with AI technologies.
- Proactively manage risks and escalations; escalate broader risks to CSTL or TA leadership as needed.
- Support budget inputs and tracking for assigned assets/studies with CSBS.
Qualifications & Experience:
- Bachelor’s degree in Pharmacy, Supply Chain Management, Business, or Pharmaceutical Sciences.
- 10+ years clinical supply chain or related operational planning/leadership experience.
- Experience across clinical, regulatory, and quality functions.
- Knowledge of all phases of drug development, relevant functions/processes, and project management principles.
- Extensive knowledge of planning, forecasting, and executing investigational materials supply strategies.
- Demonstrated ability to collaborate with and influence cross-functional teams to achieve clinical supply goals within timelines.
- Experience leading/managing change in dynamic, complex environments.
- Strong analytical and problem-solving skills; ability to monitor global clinical supply process milestones.
- Strong background in cGxPs and ICH requirements.
Compensation/Benefits (as stated):
- Starting compensation range (FTE): $159,210–$192,929 (Madison/Giralda, New Brunswick, Princeton, NJ). Additional incentive cash/stock may be available.
- Benefits include health coverage; wellbeing support programs; financial wellbeing/protection (e.g., 401(k), disability, life insurance); and paid time off (including flexible time off and national holidays; eligibility-dependent additional time off).
Application Instructions:
- If you believe the job posting is missing information required by local law or is incorrect, contact TAEnablement@bms.com with the Job Title and Requisition number (R1601463).
Key Responsibilities:
- Execute strategic vision and direction for clinical asset planning; ensure alignment of asset/study plans with established strategy and recommend improvements.
- Oversee clinical supply planning for assigned assets/studies; support continuous improvement.
- Support and guide matrix team members within assigned assets/studies; strengthen clinical supply planning capabilities.
- Serve as the single point of accountability for clinical supply planning and execution for assigned assets/studies.
- Support CSC leadership preparing materials for governing bodies and key stakeholders; provide subject-matter expertise for asset-related decisions.
- Execute CSL processes; contribute to continuous improvement using asset/study-level KPIs and performance metrics.
- Resolve issues within asset/study scope and timely escalate higher-impact risks.
- Act as primary Clinical Supply Chain point of contact for assigned compounds and studies; lead global supply strategy communications as appropriate.
- Lead matrix teams to develop and implement integrated cross-functional strategies, resourcing, and plans to ensure continuous investigational product supply and timely delivery of quality clinical supplies.
- Oversee supply forecast development for complex studies; evaluate/refine clinical development plan and protocol analysis; monitor inventory/drug utilization vs forecast, considering country requirements and logistics.
- Partner with GDO and Finance to operationalize the CD&O P process (attend Demand Alignment meetings; run Supply Review meetings).
- Assist with adoption and sustainment of a data-enabled CSL ecosystem integrated with AI technologies.
- Proactively manage risks and escalations; escalate broader risks to CSTL or TA leadership as needed.
- Support budget inputs and tracking for assigned assets/studies with CSBS.
Qualifications & Experience:
- Bachelor’s degree in Pharmacy, Supply Chain Management, Business, or Pharmaceutical Sciences.
- 10+ years clinical supply chain or related operational planning/leadership experience.
- Experience across clinical, regulatory, and quality functions.
- Knowledge of all phases of drug development, relevant functions/processes, and project management principles.
- Extensive knowledge of planning, forecasting, and executing investigational materials supply strategies.
- Demonstrated ability to collaborate with and influence cross-functional teams to achieve clinical supply goals within timelines.
- Experience leading/managing change in dynamic, complex environments.
- Strong analytical and problem-solving skills; ability to monitor global clinical supply process milestones.
- Strong background in cGxPs and ICH requirements.
Compensation/Benefits (as stated):
- Starting compensation range (FTE): $159,210–$192,929 (Madison/Giralda, New Brunswick, Princeton, NJ). Additional incentive cash/stock may be available.
- Benefits include health coverage; wellbeing support programs; financial wellbeing/protection (e.g., 401(k), disability, life insurance); and paid time off (including flexible time off and national holidays; eligibility-dependent additional time off).
Application Instructions:
- If you believe the job posting is missing information required by local law or is incorrect, contact TAEnablement@bms.com with the Job Title and Requisition number (R1601463).