Bristol Myers Squibb

General Counsel

• Prepare and prosecute patent applications, including drafting, filing, and managing responses to office actions globally
• Provide comprehensive program counseling to multiple functional areas
• Develop and implement IP strategies protecting innovations and supporting business goals
• Lead cross-functional collaboration with R&D, regulatory, commercial, and other departments
• Conduct freedom-to-operate analyses and advise on patentability and infringement issues
• Manage patent portfolios, patent landscape analyses, and patent strategies
• Support business development due diligence by evaluating IP portfolios of partners and acquisition targets
• Draft and negotiate license and research collaboration agreements
• Manage outside counsel relationships for high-quality and cost-effective legal services
• Engage business and technical teams with IP-related guidance and support
• Monitor changes in patent laws and regulations and ensure compliance
• Collaborate with in-house and outside attorneys to provide high-level legal support

Senior Patent Counsel, Innovation Law

• Prepare and prosecute patent applications, including drafting, filing, and managing responses to office actions globally
• Conduct freedom-to-operate analyses and provide strategic counsel on patentability and infringement issues
• Manage patent portfolios, conduct patent landscape analyses, and develop patent strategies to protect BMS innovations
• Provide due diligence support for business development activities by evaluating IP portfolios of potential partners and acquisition targets
• Draft and negotiate license and research collaboration agreements
• Manage relationships with outside counsel to ensure high-quality and cost-effective legal services
• Engage regularly with business and technical teams to provide IP-related guidance and support
• Monitor changes in patent laws and regulations and ensure compliance with relevant legal requirements
• Support clients across multiple functional areas and collaborate with in-house and outside attorneys

Patent Counsel, Innovation Law

General

• Promote approved indications of BMS products within the defined territory to meet or exceed assigned sales targets compliantly
• Create demand for BMS medicines by communicating the clinical and scientific rationale for use in appropriate patients
• Maintain and grow scientific expertise in assigned products and therapeutic areas
• Prepare and implement comprehensive territory and account plans
• Use CE^3 and other available tools to derive insights and inform call plans
• Present approved scientific information to HCPs through in-office presentations and lunch-and-learns
• Organize external speaker programs, including speaker selection, scheduling, and logistics
• Maintain working expertise on emerging data for approved indications
• Engage Medical on Call for unsolicited questions and complex technical inquiries
• Build and maintain credibility with regional thought leaders, community physicians, HCPs, office staff, and other patient-care stakeholders
• Collaborate with other BMS field teams and functions to improve the customer experience
• Gather and share customer insights internally with appropriate stakeholders
• Comply with all laws, regulations, and BMS policies
• Spend 100% of time in the field with external customers

Senior Therapeutic Area Specialist, Oncology

Consultant

• Develop and maintain relationships with academic and community health care professionals within the assigned geography
• Provide clinical and product education for BMS hematology and oncology products through 1:1 interactions, group presentations, and remote channels
• Assess treatment and patient management landscapes, needs, and current processes/protocols
• Use approved on-label CNC resources and presentations while ensuring accuracy and compliance
• Evaluate the impact of CNC activities and plan follow-up or next steps
• Respond and adapt to educational gaps and customer needs
• Monitor CNC dashboard and account data and adjust activities and business plans
• Maintain knowledge of treatment landscapes, product attributes, and disease states
• Deliver educational speaker programs in approved out-of-office settings
• Deliver educational in-services for HCP customers
• Provide product demonstrations and infusion support for CAR T sites starting new patients
• Support clinical, disease-area, and product-specific training for internal stakeholders
• Participate in assigned Medical Congress activities
• Share clinical insights and patient-management experiences internally to support franchise strategy
• Develop relationships with hematology- or oncology-focused Patient Support Groups and present approved educational materials as needed

Clinical Nurse Consultant

Director

• Lead PDS’s strategic intelligence and insights capability
• Monitor internal and external market, geopolitical, regulatory, supply chain, and organizational developments
• Establish early-warning sensing mechanisms for emerging issues and opportunities
• Synthesize information across PDS operating units and external sources to identify patterns, interdependencies, risks, and business implications
• Translate complex data, trends, and signals into concise insights, scenarios, and actionable recommendations
• Build and sustain stakeholder networks across PDS, Enterprise Risk Management, enterprise functions, business partners, and the GSC triage team
• Consolidate internal perspectives and external intelligence into a unified strategic picture
• Develop executive-ready briefings, presentations, and decision-support materials
• Support or directly brief leadership forums, governance reviews, and enterprise discussions
• Assess emerging issues and recommend proactive responses
• Partner with Enterprise Risk Management, Strategy, and governance organizations
• Create standardized intelligence products, reporting formats, and analytical frameworks
• Refine sensing methodologies, source networks, and insight-generation processes
• Report into the Strategic Realization and Governance pillar as an individual contributor

Associate Director, Strategic Intelligence, Insights

• Co-lead complex, enterprise-level initiatives with business leaders by establishing problem statements, outcomes, decision rights, governance, and integrated roadmaps
• Connect functions around dependencies and trade-offs and maintain cadence for decisions, risks, and progress
• Lead highest-priority PDS initiatives end-to-end from hypothesis framing and assumption testing through mobilization and execution enablement
• Define workstreams, milestones, owners, success measures, and strategic levers required to deliver value
• Translate business intelligence and external market signals into implications for growth, performance, and strategic direction
• Synthesize findings into scenarios and recommendations and brief senior and executive leaders
• Lead cross-functional program teams through operating rhythms, governance forums, decision tracking, dependency management, benefit measures, and escalation paths
• Structure ambiguous problems by gathering evidence, testing hypotheses, and developing practical frameworks, options, and recommendations
• Partner with senior functional leaders to drive rigorous analysis of complex datasets and business processes
• Develop executive communications including decision briefs, steering updates, and leadership narratives
• Serve as escalation point and advisor on program risk, prioritization trade-offs, and resourcing decisions
• Build an inclusive team environment supporting collaboration, strategic program leadership capability-building, and professional growth

Senior Director, Strategic Program Delivery

• Collaborate in the design of innovative and efficient clinical trials, including study population and endpoint selection
• Contribute to project development strategy
• Defend protocols and analysis plans at internal governance reviews
• Independently author and/or review protocols, statistical analysis plans, clinical study reports, publications, and other study-level documents
• Present summary data and analyses clearly, concisely, completely, and transparently
• Provide statistical support and leadership for health authority requests, publications, presentations, and public release of information
• Manage multiple studies to ensure consistency and adherence to standards within an indication or therapeutic area
• Apply statistical and clinical trial methodology to clinical development
• Develop knowledge of clinical, regulatory, and commercial environments and apply it to study design
• Engage as a matrix team member and scientific and strategic partner in drug development
• Comply with BMS processes, SOPs, global standards, and project standards
• Contribute to internal and external statistical communities of practice
• Develop and advise team members
• Communicate the DQS Mission and Vision
• For people managers: advocate for employees, coach and mentor team members, provide leadership, guide development plans, conduct performance reviews, provide feedback, and develop staff performance metrics

Associate Director, Biostatistics

• Own the technology roadmap and lifecycle for Automated QC equipment and software, including upgrades, vendor management, and long-term platform planning
• Lead deployment of Automated QC systems at new and existing nodes across the Cell Therapy manufacturing network
• Sequence and coordinate priorities across concurrent programs
• Partner with Assay and Data Automation and Analytical Sciences and Technology to define system requirements, validate performance, and resolve technical issues
• Serve as primary point of contact for receiving sites and ensure operational and quality readiness before go-live
• Represent Automated QC strategy and progress in network-level technical and governance forums
• Identify deployment or system-performance risks and drive mitigation plans
• Ensure systems and processes meet cGMP requirements
• Support regulatory filings as needed
• Establish key performance metrics and report deployment progress to stakeholders and leadership
• Lead, coach, and develop the team supporting deployment and sustaining operations

Director, QC Automation

• Provide strategic leadership and oversight of the Protocol Management Office (PMO)
• Lead review of clinical protocols, statistical analysis plans (SAPs), Data Monitoring Committee (DMC) charters, and other critical study documents across the BMS portfolio
• Provide scientific review, commentary, and revision of pivotal protocols and documents across all therapeutic areas
• Oversee coordination of review activities and align resources with required activities
• Liaise with senior Drug Development stakeholders and support consistent review processes
• Ensure studies meet scientific quality, feasibility, regulatory, and compliance standards
• Develop and refine protocol/document submission processes and triage criteria
• Integrate review processes into overarching governance processes
• Maintain compliant systems for storing and retrieving review materials, meeting outputs, and decisions
• Develop metrics and indicators for protocol development and continuous improvement
• Incorporate advances and external insights into protocol development and study design
• Lead educational and training programs for clinical physicians and scientists
• Develop training materials with BMS Learning
• Contribute to a best-practices hub and nurture internal knowledge-sharing communities
• Lead initiatives enhancing clinical development innovation and efficiency
• Oversee clinical process development, maintenance, measurement, and compliance
• Contribute to Clinical Development Plan (CDP) and Integrated Asset Development Plan (IADP) processes
• Partner with Data and Quantitative Sciences and Real World Data Research/IT to use real-world evidence and AI in trial design
• Streamline the study design and protocol development journey
• Collaborate with Global Quality and Risk Based Management to embed Quality by Design and critical-to-quality factors
• Serve as Global Process Owner for Protocol development within the QMS network
• Evaluate and implement industry-leading capabilities and enterprise initiatives
• Lead implementation of AI and technology, including FARO, to optimize protocols and reduce patient/site burden, cost, and amendments
• Monitor KPIs for innovative protocol and protocol-process solutions
• Evaluate cross-functional ways of working across the OneClinical model
• Foster innovation, collaboration, customer focus, accountability, and commitment to results
• Report to the SVP, Head of Drug Development Strategy & Innovation

Executive Director – Head of Clinical Design & Delivery Center

Events

• Support complex microbiological and sterility assurance investigations at internal manufacturing sites, including environmental monitoring excursions, sterility test failures, and process-related contamination events
• Serve as MQSA SME for microbiological and aseptic process impact assessments
• Evaluate root cause analyses and assess product, process, and patient impact
• Review and formally sign off on investigation reports, CAPA records, and deviation documentation
• Partner with site Investigation Leads on investigation scope, RCA depth, and CAPA effectiveness
• Lead rapid containment and triage for sterility breaches, leaks, mold recoveries, and contamination events
• Track and trend impact assessment outcomes to identify systemic issues and emerging risks
• Support regulatory agency inspections and audits related to impact assessments and sterility assurance
• Act as technical liaison for External Manufacturing partners on sterility and microbiological investigations
• Review ExM investigation reports and impact assessments and provide feedback
• Support CMO quality risk assessments and periodic reviews of aseptic operations, contamination control programs, and microbiological trends
• Design and implement CMO oversight tools, dashboards, and decision trees
• Participate in remote and on-site CMO technical reviews, site assessments, vendor selection, and external manufacturing audits
• Provide expertise in aseptic processing, barrier technology, cleanroom design, gowning programs, and aseptic technique qualification
• Support media fills, process validation, revalidation, contamination control strategies, and aseptic process change controls
• Support cGMP improvements and regulatory guidance interpretation
• Consult on microbial sampling during technology transfers and qualification activities
• Author and approve CMC process validation P.3.5 documentation
• Support CMC queries with Global Health Authorities and plant inspections
• Mentor site-level microbiologists and quality professionals
• Develop and maintain global MQSA standards, SOPs, guidance documents, and training materials
• Monitor industry trends, regulatory updates, and scientific literature
• Represent MQSA in cross-functional teams, steering committees, and governance forums
• Interface with BPOG, ISPE, PDA, and similar industry consortiums

Senior Manager, Internal Contamination Events & Investigations

Machine Learning Engineer

• Lead and grow a team of machine learning scientists focused on ADMET/PK prediction and multiparameter design for small molecules
• Set scientific strategy and priorities for the Machine Learning Sciences team
• Partner with computational scientists, medicinal chemists, DMPK scientists, in vitro biologists, and data scientists
• Embed ML-driven predictions into project workflows and decision-making
• Drive model predictivity improvements through validation, benchmarking, and iteration against experimental data
• Evaluate academic literature, startups, platforms, and emerging technologies
• Lead assessment and adoption of promising approaches into predictive workflows
• Represent Machine Learning Sciences in cross-departmental forums
• Communicate results, capabilities, and strategy to scientific and senior leadership
• Mentor and develop team members
• Contribute to departmental strategy as a member of the Computational Sciences leadership community
• Report to the Executive Director of Small Molecule Computational Sciences

Associate Director – Machine Learning Sciences

• Promote approved indications of BMS products within a defined territory or region to meet or exceed sales targets compliantly
• Create demand for BMS medicines by explaining the clinical and scientific rationale for use in appropriate patients
• Maintain and grow scientific expertise in assigned products and therapeutic areas
• Prepare and implement comprehensive territory and account plans
• Use tools such as SOPHIA to derive insights and dynamically inform call plans
• Provide feedback on tools to leadership for continuous improvement
• Present approved scientific information to HCPs through in-office presentations and lunch-and-learns
• Organize external speaker programs, including speaker selection, scheduling, and logistics
• Maintain expertise on emerging data for approved indications
• Use Medical on Call for unsolicited questions and complex technical inquiries
• Collaborate with other field teams to provide the best Customer Experience
• Gather and share customer insights internally with appropriate stakeholders
• Liaise with BMS functions to meet HCP needs in a timely and scientific manner
• Prioritize safe and appropriate use of BMS products while achieving business objectives
• Build and maintain credibility with regional thought leaders, community physicians, HCPs, office staff, and other patient-care stakeholders
• Spend much of the time in the field with external customers
• Comply with laws, regulations, and BMS policies

Senior Therapeutic Area Specialist, Cardiovascular Specialty

Research Scientist

• Apply radiopharmaceutical-specific modeling expertise to research and development of new drugs and therapies
• Perform radiopharmaceutical dose modelling and analyze in vitro and in vivo, clinical diagnostic, and therapeutic study data
• Lead translational dosimetry analyses, including physiologically based pharmacokinetic and compartmentalization modelling
• Provide technical support, dosimetry calculations, training, and problem-solving solutions to cross-functional teams
• Collaborate with internal stakeholders, external vendors, and subject-matter experts
• Support internal dosimetry analysis for discovery and development of radiopharmaceutical imaging and therapeutic agents
• Design experiments and analyze dosimetric data from PET and SPECT imaging to assess drug uptake and distribution
• Advise on best practices and standardization for image data quality control in preclinical research
• Analyze preclinical and clinical imaging data to advance animal-to-human dose projection
• Explore new technologies and modelling approaches, including novel radioisotopes such as alpha-emitters
• Contribute to medical physics knowledge in radiopharmaceuticals
• Apply AI to improve team execution and decision-making

Principal Scientist, Medical Physicist

Vice President

• Define and drive the long-term global external manufacturing strategy across BMS portfolios
• Create a clinical development through commercial manufacturing operating model
• Align external manufacturing capacity with pipeline progression and commercial demand forecasts
• Develop contingency plans and strategic optionality
• Own and drive the AI and digital strategy for the external manufacturing network
• Enable real-time, bidirectional data exchange with CMO/CDMO partners
• Establish an AI governance framework for the external manufacturing ecosystem
• Build digital infrastructure and data architecture across 75+ external partners
• Provide business, relationship, and operational oversight of 75+ external partners globally
• Build and sustain a flexible, agile external manufacturing network
• Lead Supplier Relationship Management models and virtual plant team structures
• Develop, negotiate, implement, and enforce supply contracts with external parties
• Hold ultimate accountability for GMP compliance and health authority inspection readiness
• Identify network risks and ensure escalation and stakeholder communication
• Ensure reliable, on-time, and predictable product delivery
• Set and track financial goals for external manufacturing partners
• Drive continuous improvement, issue resolution, network resilience, business continuity, and COGS reduction
• Lead, inspire, and develop an inclusive organization of 600+ professionals globally
• Identify future talent and workforce needs; hire and develop change agents
• Lead transformative opportunities and organizational change
• Partner with Quality, Regulatory, MS&T, Supply Chain, Procurement, Product Development, and Finance
• Serve as the primary enterprise voice for External Manufacturing at senior leadership level
• Advise the EVP, Chief Supply Chain & Operations Officer
• Collaborate with and participate on matrix leadership teams

Vice President, External Manufacturing

• Lead the pooled Senior Manager, Agile Strategic Learning Partner team and hold direct line-management responsibility
• Define and operationalize agile pooled resourcing mechanics, capacity matching, portfolio review rhythms, and skills-based resourcing
• Ensure projects complete standardized intake before resourcing is considered
• Apply independent Priority, Tier, and Resource criteria across the portfolio
• Maintain and present the CoE Book of Work
• Match Senior Managers to projects based on skills, specialist knowledge, capacity, and project phase
• Lead portfolio reviews to rebalance capacity and resolve over- or under-capacity issues
• Uphold operating guardrails, including prototype-focused work, LEAP handoff for systematized production, and a 70% strategy/30% creation target
• Partner with functional Associate Directors to align pooled resources with priorities and maintain a coherent learner experience
• Collaborate with LEAP on requirements, SME nominations, review cycles, delivery readiness, performance reporting, value validation, and vendor governance
• Partner with HR and IT on AI- and technology-enabled workforce design and operating model approaches
• Track operating model indicators such as intake tiering, prototype turnaround, workload ratios, capability uplift, reuse, and cost avoidance
• Report portfolio health and active demand pipeline to the Senior Director and governance forums
• Stay current on AI-enabled learning technologies and recommend scalable practices