Description:
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 .
The Senior Director, Clinical Supply Team Lead is a strategic and operational
leader accountable for end to end clinical supply activities execution across
an assigned Therapeutic Area (TA). This role ensures seamless delivery of
investigational products by overseeing planning, forecasting, resourcing, and
operational performance across all studies and assets within the TA.
The Clinical Supply Team Lead directs Clinical Supply Leads (CSL), Trial
Supply Managers (TSMs), and other team members by balancing workload,
resolving operational conflicts, and achieving operational excellence by
driving execution and accountability. The leader partners closely with cross
functional teams, including GDO, CMC, Regulatory, Quality, GLS, CSO, and
Finance, to promote collaboration and strategic foresight as well as to
anticipate demand, manage risk, allocate resources, and ensure alignment
with clinical development priorities.
This role also serves as a key contributor to CSC's digital, analytical, and
continuous improvement agenda leveraging data, AI enabled insights, and
standardized processes/playbooks to strengthen supply chain reliability,
reduce risk, and improve speed for patients. This role also supports the
development of future-ready talent within their assigned TA.
Key Responsibilities
Provide strategic direction and operational leadership across all studies and assets (including integrations) within the TA, ensuring alignment with protocol needs, regulatory requirements, and organizational goals/priorities.
Facilitate regular strategic discussions with TA Leads and stakeholders to ensure alignment, rapidly resolve issues, anticipate resource swings, and share forward-looking insights.
Serve as the TA's primary point of coordination for new assets, new studies, and incoming work, ensuring rapid assessment, appropriate coordination, and structured assignment paths.
Coordinate and oversee TA-level capacity planning, balancing SAL, TSM, and IPC workload across the portfolio and across CSC to avoid bottlenecks, mitigate risks, and ensure timely support.
Leverage Control Tower / E2E supply data and processes to anticipate workload shifts, demand spikes, resourcing needs, and performance trends, as well as take proactive steps to address CSC opportunities and mitigate risks.
Lead the intake process for all new requests (CMC, GDO, IRT, etc.), including chairing intake meetings and making SAL/TSM assignment decisions based on expertise, capacity, study prioritization, and other relevant managerial/operational factors.
Act as first-line decision-maker for cross-study or cross-asset conflicts, study prioritization, escalation/acceleration handling, and trade-off alignment across the TA and between TAs, as needed.
Anticipate risks and proactively intervene or escalate to avoid near misses, delays, or supply disruptions across the TA. Lead root cause analyses when misses, delays, or supply disruptions occur.
Serve as the TA's senior representative during portfolio reviews, scenario planning, pipeline acceleration discussions, and integration activities (e.g., due diligence, new modalities).
Contribute to improving CD&OP maturity by reinforcing consistent inputs, process discipline, and cross-functional engagement. More tactically ensure the appropriate projects are being escalated up the CD&OP process to achieve rapid resolution.
Own creation, monitoring, analysis, reporting, and evolution of common CSC KPIs, leadership dashboards and performance metrics to identify and act upon emergent trends, bottlenecks, changed assumptions, changed scope, and other managerial signals.
Drive data-enabled decision-making, leveraging AI-enabled insights and validated data sets to guide operational improvements, assess resource allocations and inform timely, actionable future planning.
Partner with other TA Ops Leads to ensure intra- and inter-TA harmonization, alignment, coordination, continuous improvement.
Oversee TA-level compliance to GxP, Quality, and regulatory inspection expectations ensuring SALs, TSMs, and other staff maintain timely and accurate data, forecasts, systems, and documentation.
Provide guidance, coaching, accountability, and mentoring to SALs, TSMs, and other team member; build a future-ready skill portfolio across the TA (digital fluency, data analysis, strategic thinking).
Qualifications & Experience
Bachelor's degree in Pharmacy, Engineering, Supply Chain, Life Sciences, or related field.
15+ years of clinical supply chain, clinical operations, technical operations, or related biopharmaceutical leadership experience.
Demonstrated expertise in end-to-end clinical supply planning, investigational product management, and global study execution.
Demonstrated strategic planning and leadership skills.
Knowledge of effective executive communications, stakeholder management, and partner/customer engagement.
Strong understanding of drug development, clinical operations, CMC, regulatory expectations, and GxP quality systems.
Proven ability to lead matrixed teams, manage senior stakeholders, and influence without authority across global and cross-functional environments.
Advanced analytical skills with experience using digital tools, dashboards, AI-enabled insights, or supply chain performance data.
Demonstrated success providing change leadership within dynamic, complex, fast-paced environments.
Ability to recruit, select, coach, engage, and develop team members.
| Organization | Bristol Myers Squibb UK & Ireland |
| Industry | Management |
| Occupational Category | Senior Director |
| Job Location | Dublin,Ireland |
| Shift Type | Morning |
| Job Type | Full Time |
| Gender | No Preference |
| Career Level | Department Head |
| Experience | 15 Years |
| Posted at | 2026-04-17 9:31 pm |
| Expires on | 2026-06-01 |