Director, Clinical Supply Lead (CSL)
Bristol Myers Squibb
8 hours ago
Remote friendly (New Brunswick, NJ)
United States
Operations
Director, Clinical Supply Lead (CSL)
Responsibilities
- Lead TA-level intake and planning for new studies/assets and major protocol changes, coordinating IRT awareness, comparator needs, and supply requirements.
- Provide matrix leadership to oversee intra-study CSLs, TSMs, and CSC team members (capacity, expertise, study tiering).
- Establish decision-making framework; coach and hold accountable the asset matrix team.
- Serve as main contact for assigned compound/studies; manage global supply strategy communications.
- Resolve conflicts/trade-offs/risks; drive standardized processes/playbooks, escalation pathways, and governance expectations.
- Lead cross-functional integrated strategies, resourcing, and implementation plans to ensure continuous investigational product supply.
- Oversee complex supply forecasts; monitor inventory and utilization vs forecast (country/logistics aware).
- Provide input for program-level planning/distribution; align CSC staffing and tactical execution with supply strategies.
- Execute/lead CSL processes and drive continuous improvement using performance data/KPIs; partner with GLS/CSC planning for supply reliability.
Qualifications
- Bachelor’s degree (supply chain, Pharmacy, Life Sciences, Engineering, or related).
- 12+ years’ experience in clinical/technical operations or clinical supply chain.
- GxP planning/forecasting/operational leadership; strong cross-functional influencing.
- Knowledge of investigational product supply, study operations, and interfaces (CMC/Regulatory/Quality/GDO).
Preferred
- Clinical supply chain professional management; supply planning/S&OP (CD&OP desirable); digital tools (IBP, Lighthouse, Control Tower, CASSA); portfolio/multi-study coordination.
Benefits (explicitly listed)
- Medical/pharmacy/dental/vision; wellbeing programs; 401(k), disability, life/accident insurance, etc.; paid time off (flexible time off or annual vacation per location).
Responsibilities
- Lead TA-level intake and planning for new studies/assets and major protocol changes, coordinating IRT awareness, comparator needs, and supply requirements.
- Provide matrix leadership to oversee intra-study CSLs, TSMs, and CSC team members (capacity, expertise, study tiering).
- Establish decision-making framework; coach and hold accountable the asset matrix team.
- Serve as main contact for assigned compound/studies; manage global supply strategy communications.
- Resolve conflicts/trade-offs/risks; drive standardized processes/playbooks, escalation pathways, and governance expectations.
- Lead cross-functional integrated strategies, resourcing, and implementation plans to ensure continuous investigational product supply.
- Oversee complex supply forecasts; monitor inventory and utilization vs forecast (country/logistics aware).
- Provide input for program-level planning/distribution; align CSC staffing and tactical execution with supply strategies.
- Execute/lead CSL processes and drive continuous improvement using performance data/KPIs; partner with GLS/CSC planning for supply reliability.
Qualifications
- Bachelor’s degree (supply chain, Pharmacy, Life Sciences, Engineering, or related).
- 12+ years’ experience in clinical/technical operations or clinical supply chain.
- GxP planning/forecasting/operational leadership; strong cross-functional influencing.
- Knowledge of investigational product supply, study operations, and interfaces (CMC/Regulatory/Quality/GDO).
Preferred
- Clinical supply chain professional management; supply planning/S&OP (CD&OP desirable); digital tools (IBP, Lighthouse, Control Tower, CASSA); portfolio/multi-study coordination.
Benefits (explicitly listed)
- Medical/pharmacy/dental/vision; wellbeing programs; 401(k), disability, life/accident insurance, etc.; paid time off (flexible time off or annual vacation per location).