Bristol Myers Squibb

Director

• Lead and manage a team of analytical Subject Matter Experts (SME) responsible for the commercial drug product release methods utilized in the cellular biology, molecular and flow cytometry areas.
• Provide technical oversight and guidance to team as needed in support of method performance troubleshooting, evaluation of analytical test methods and data generated by internal and external laboratories, including investigations related to out of specification, out of trend, and aberrant results.
• Oversee method performance metrics and the team’s completion of quality events including actions and investigations within electronic systems.
• Act as a Subject Matter Expert (SME) in functional areas as needed.
• Partner with analytical development and the commercial QC organization to identify method optimization and automation opportunities to enhance productivity and reduce the cost of product testing.
• Interface with analytical development functions on method qualification strategies.
• Hire, mentor, and develop exceptional ASAT personnel.

Associate Director, Drug Product Analytical Science and Technology

Research Scientist

• The Principal Scientist is a highly experienced subject matter expert responsible for leading method optimization, transfer, and validation in support of Cell Therapy analytical portfolio.
• Conceptualize and lead complex projects, provides strategic scientific and technical input to the programs and projects.
• Apply technical knowledge, regulatory requirements, and scientific principles to independently perform complex troubleshooting and problem solving.
• Balance deep hands-on laboratory involvement with cross-functional leadership, mentoring, and external scientific engagement.
• Represent the department in product review boards, regulatory inspections (internal and external audits).
• Own and author relevant analytical sections of regulatory submission and responses to health authority questions and requests.

Principal Scientist, Analytical Science and Technology, Cell Therapy

Data Scientist

• Frame ambiguous business and scientific questions into measurable AI product hypotheses, success metrics, evaluation plans, and rapid experiments.
• Contribute to six-sprint, 12-week AI Accelerator agile cycles by testing hypotheses, validating AI product increments, and adapting analyses during two-week sprints.
• Build data science prototypes using Python, SQL, notebooks, APIs, and AWS-aligned data services.
• Support sandboxed data problem solving in non-production environments, enabling agents and analysts to branch, transform, test, and audit code-plus-data experiments before promotion.
• Evaluate and curate the analytical context agents and analysts rely on, including explicit instructions, memory, data tools, and curated meaning from source materials and recommend improvements based on measured impact on agent quality.
• Develop analytical features, embeddings, classifiers, ranking/scoring methods, recommendation logic, simulation approaches, or optimization methods as needed for product outcomes.
• Partner with Data Engineers to shape reliable datasets, retrieval corpora, metadata, and feature pipelines using S3, Athena, PostgreSQL/RDS, vector databases, and knowledge graphs.
• Design and execute evaluations for LLM, RAG, and agentic workflows, with emphasis on context quality, knowledge curation, semantic evolution, and model quality.
• Build evaluation rubrics, golden datasets, structured output validation, error taxonomies, hallucination risk measurement, and SME review loops.
• Use tools such as LangGraph, LangSmith, PydanticAI, or similar frameworks to test agent behavior, retrieval quality, reasoning traces, and workflow reliability.
• Evaluate whether curated enterprise context improves agent quality, reliability, traceability, and decision usefulness compared with raw document retrieval.
• Assess model and agent outputs for quality, uncertainty, calibration, bias, hallucination risk, traceability, and fitness for intended use.
• Explore approved proprietary and open model options through enterprise channels and recommend model/task pairings based on evidence, risk, cost, and performance.
• Define KPIs and analytical measurement plans for AI products, including adoption, user behavior, workflow efficiency, scientific utility, and business value.
• Use bi-weekly demos, sprint reviews, stakeholder feedback, and performance results to measure MVP progress and assess readiness for scaling or production transition.
• Apply statistical modeling, experimental design, causal inference, or quasi-experimental methods where appropriate to separate signal from noise.
• Create clear analyses, visualizations, and narratives that help product teams and stakeholders understand model behavior, limitations, and opportunities.
• Partner with responsible AI, security, quality, and domain experts to ensure evaluations and analytics respect data privacy, scientific integrity, and enterprise governance.
• Contribute reusable notebooks, context-quality evaluation harnesses, analytics templates, prompt/evaluation assets, and data science patterns that can be adopted across pods.
• Participate in code reviews, analysis reviews, design discussions, and technical problem-solving with engineering and product teams.
• Use coding agents and AI-assisted development tools effectively while validating outputs, documenting assumptions, and maintaining scientific rigor.
• Continuously refine analytical priorities and backlogs as insights emerge, incorporating stakeholder input, performance results, and lessons learned throughout MVP development.
• Coach peers on practical data science, evaluation design, measurement strategy, and evidence-based decision making in fast-moving AI delivery environments.

Senior Data Scientist

Therapist

• Provide bioassay, flow cytometry and/or molecular biology analytical expertise in support of QC lab investigations.
• This encompasses supporting technical investigations to identify root cause and provide corrective and preventive actions, including method remediations and experimental studies at the bench.
• In accordance with established protocols and research objectives, independently execute experimental work with a high degree of technical proficiency, contribute to data analysis and documentation, and collaborate within cross-functional teams.
• Contribute to the development and optimization of new and existing laboratory methods and protocols.
• Present experimental findings and progress updates to immediate team.
• Support the preparation of internal technical reports and presentations as appropriate.
• Support transfer of commercial methods and method validation in compliance with global regulatory requirements.
• Responsible for the stewardship of bioassay, flow cytometry and/or molecular methods in the Cell Therapy Quality organization.
• Implement method lifecycle and method maintenance programs to support bioassay, flow cytometry and/or molecular biology methods in support of cell therapy drug products.
• Author, revise, and review technical documents such as test methods, SOPs, trend reports, and/or investigation reports as appropriate.
• May lead project, CAPA and deviation/investigation related tasks and/or continuous improvement efforts.
• May provide support in the authoring of the analytical sections of regulatory submissions, responding to health authority questions and functioning as the method validation and method transfer expert during inspections as required.
• May partner with development organizations in the design of development and qualification studies, selection and characterization of reagents, and method optimization initiatives.
• Perform other tasks as assigned.

Scientist, Analytical Science and Technology – Cell Therapy

Operations

• The MSL is responsible for identifying disease and product related medical needs in a defined geography.
• The primary role of the MSL is to develop and maintain relationships with Thought Leaders (TL) and Healthcare Providers (HCP) within their territory.
• Engage in meaningful scientific exchange that will ensure patients have access to BMS medicines.
• Facilitate research and serve as the medical resource for external stakeholders in the community.
• Develop geography-specific Field Medical and TL Interaction plans based on therapeutic area objectives and TLs needs.
• Adopt institution/account planning approach and contribute to cross-functional institution/account plans.

Medical Science Liaison, Neuropsychiatry

Risk

• Develop the Quality Narrative (or equivalent) at a study and/or ASSET and TA level, to document the end-to-end risk-based quality management for CtQ data, processes and vendors demonstrating effective risk and issue management.
• Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback loop to ensure mitigation strategies are adjusted when new or unanticipated issues arise once the trial has begun.
• As part of the upstream protocol authoring process, partner with Drug Development to embed Quality by Design principles and help identify study specific critical to quality (CtQ) data, processes and vendors and ensure adequate risk mitigation strategies have been implemented.
• During trial conduct, provide feedback on risks to study specific critical to quality factors and ensure mitigation strategies are adjusted when new or unanticipated issues arise once the trial has begun.
• Conduct spot checks to ensure risk mitigation strategies are accurately translated into operational plans.
• Assist the business in defining and establishing Acceptable Ranges/QTL and KRIs for CtQ data.
• Provide regulatory intelligence on current and upcoming regulations to ensure we remain compliant with all applicable requirements.
• Support the monitoring and evaluation of CtQ factors throughout the study lifecycle and adapt Quality plans accordingly.
• Provide R&D Quality expertise, critical thinking, deliver training and share best practices and lessons learned into future trials.

Associate Director, Quality Risk Management

Manager

• Ensure that analytics assets (data models, ML, AI, and DI) are reliably and efficiently deployed and maintained in production.
• Set up continuous integration pipelines to automate the testing, validation, and deployment of analytics assets.
• Implement automated monitoring and alerting systems to ensure that any disruptions or anomalies in the analytics assets are promptly addressed.
• Collaborate with data engineers and scientists to understand data and model requirements and ensure seamless integration into production systems.
• Troubleshoot and resolve complex issues related to deployment, performance, and scalability.
• Develop governance policies for data management, model development, and analytics deployment.
• Scale best practices across the organization to ensure consistency and efficiency.
• Implement robust security measures to protect data assets.
• Participate in decision making and brings a variety of strong views and perspective to achieve team objectives.
• Demonstrate a focus on improving processes, structures and knowledge within the team.
• Lead in analyzing current states, deliver strong recommendations in understanding complexity in the environment, and the ability to execute to bring complex solutions to completion.
• Stay up-to-date with the latest trends and advancements in MLOps and machine learning technologies.

Senior Manager, Knowledge Systems

• Partner with Statistics Therapeutic Area leadership to develop and execute strategic plans aligned with portfolio priorities.
• Drive consistency and excellence in operational processes, while creating an environment of data-driven decision-making.
• Lead cross-functional project delivery from ideation to execution, ensuring transparency, accountability, and measurable outcomes, with change management and value realization embedded throughout.
• Oversee end-to-end financial planning and reporting, including budget projections, vendor spend tracking, and risk management.
• Monitor and optimize resource allocation for internal and external teams, supporting both pipeline objectives and continuous improvement efforts.
• Facilitate strategic discussions, escalate key risks, and collaborate with project leads across the organization.
• Work with technical leads to manage reporting, compliance, and KPIs, following best practices.
• Lead or support continuous improvement initiatives focused on process optimization and technical innovation.
• Author leadership messaging and change management communications for internal and external stakeholders.
• Mentor junior talent in best practices for project management, stakeholder engagement, and continuous improvement.
• Build and maintain strong relationships across divisions, fostering collaboration and knowledge sharing.
• Coordinate internal events (e.g., Townhalls, scientific innovation meetings) and conference management activities.
• Ensure adherence to company policies, regulatory requirements, and quality standards.

Associate Director, Strategy and Operations

• Serves as a primary source of medical accountability and oversight for multiple clinical trials
• Matrix management responsibilities across the internal and external network
• Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities
• Provides medical and scientific expertise to cross-functional BMS colleagues
• Leads medical data review of trial data, including eligibility review
• Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines)
• Holds responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives
• Leads collaboration with CS and inputs into protocols, providing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related clinical considerations)
• Fulfills GCP and compliance obligations for clinical conduct and maintains all required training
• In collaboration with the Clinical Development Lead, designs and develops clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets
• Provides oversight and medical accountability for a group of studies
• Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working with Clinical Scientists (CS)
• Partners with CS to support executional delivery of studies (e.g., site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc.)
• Identifies and builds relationships with principal investigators. Identifies and cultivates thought leaders in order to gain their inputs on emerging science in drug and biomarker research, disease knowledge, and design of clinical development studies and programs
• Maintains a strong medical/scientific reputation within the disease area. Has in-depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder.
• Holds strong expertise in the disease area by attending scientific conferences and ongoing review of the literature
• Keeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscape
• Provides ongoing medical education in partnership with collaborating Clinical Scientists to allow for protocol-specific training, supporting the study team, investigators, and others

Director, Global Clinical Physician – Neuroscience

Data Engineer

• Partner with discovery, translational, clinical, computational, and portfolio scientists to identify high-value research opportunities for AI and translate them into AI-tractable specifications with measurable scientific success criteria.
• Architect, build, and operationalize agentic and multi-agent workflows for complex scientific tasks such as target evidence assembly, indication rationale construction, biomarker interpretation, translational synthesis, literature and evidence triangulation, and decision support.
• Design reusable AI capabilities, including agentic frameworks, evaluation harnesses, MCP-enabled tool integrations, prompt and policy libraries, and research workflows intended for adoption across multiple programs rather than single-use deployments.
• Establish rigorous evaluation methodologies for AI-enabled research outputs and upstream data/tool quality, including expert-reviewed benchmarks, rubric-based assessments, grounding checks, uncertainty characterization, provenance review, reproducibility criteria, longitudinal monitoring, and failure-mode analysis.
• Operate with urgency and tight scientific feedback loops, converging with scientists on working artifacts quickly and pivoting based on direct evidence, evaluation results, and stakeholder input.
• Collaborate with engineering, data, IT, security, legal, vendor, and platform teams to ensure AI capabilities are designed with appropriate governance, integration paths, productionization patterns, and credible scaling plans from inception.
• Communicate AI opportunities, risks, limitations, evaluation outcomes, and recommended decisions clearly to scientific, technical, and executive audiences; contribute to internal standards, reference implementations, and documentation.
• Stay current with developments in agentic systems, evaluation methodology, reasoning models, retrieval, grounding, biomedical AI tooling, and research informatics, and assess where they create practical value for Research.

Senior Scientific Data Engineer

Community Manager

• Promotes approved indications of BMS products within a defined territory or region to meet or exceed assigned sales targets in a compliant manner.
• Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients.
• Engages with and continuously maintains/grows a high level of scientific expertise in all assigned products and therapeutic areas.
• Prepares and successfully implements comprehensive territory and account plans.
• Proactively uses available tools such as SOPHIA to derive insights and to dynamically inform call plans.
• Provides feedback on experience using these tools to leadership to enable continuous improvement.
• Demonstrates scientific expertise and passion in using approved scientific resources and publications to present information to HCPs and ensures medical accuracy.
• Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label.
• Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics.
• Maintains a high level of working expertise on emerging data for approved indications.
• Engages real-time medical support through Medical on Call to reactively answer unsolicited questions and complex technical inquiries.
• Proactively collaborates with other field teams to ensure the best Customer Experience (Cx) for HCPs.
• Gathers and shares relevant insights and information internally with the appropriate stakeholders to enable BMS to better serve its customers.
• Complies with all laws, regulations, and policies that govern the conduct of BMS.

Senior Therapeutic Area Specialist, Cardiovascular

• Accountable for the clinical contribution to the development of each indication strategy, including registrational and non-registrational studies, with the support of the CTPs and Clinical Scientists (CS) within the asset and/or indication
• Responsible for managing clinical trial physician(s); attracting, developing and retaining top talent; ensuring appropriate training and mentoring of clinical trial physicians
• May serve as CTP as necessary
• Accountable in partnership with the Clinical Scientist for the design, execution, and analyses of each study led by the CTPs and CSs. Should work to proactively partner with these roles
• Accountable for clinical content for CSRs, regulatory reports, briefing books and submission documents
• Champions a quality-focused mindset and ensures adherence to GCP and compliance obligations for clinical conduct
• Represents Clinical Development in both internal and external forums as the consulted authority for the disease area, including within Business Development function
• Partners with Worldwide Patient Safety physicians in the ongoing review of safety data
• Serves as the (co-)leader of the cross-functional Clinical Development Team
• Provides clinical leadership and disease area expertise into integrated disease area strategies
• Partners closely with KOLs in specific indications
• Serves as Primary Clinical Representative in Regulatory interactions
• Evaluates strategic options against a given Target Product Profile (TPP)
• Collaborates with Global Development Operations/Global Compliance Group to develop asset level risk management plan, resolves issues with Quality/CS, and raises to DT as needed
• Sets executional priorities and partners with CTP and CS to support executional delivery of studies
• Accountable for top line data with support of CTP, CS, and Statisticians

Senior Director, Global Clinical Development – Oncology

Program Manager

• Collaborate with the ICN Translational Medicine Lead to design and execute comprehensive program timelines, integrating scientific and operational expertise to deliver translational biomarker strategies.
• Oversee key activities, including data delivery, contracting, data transfers, regulatory submissions, and internal/external collaborations
• Provide strong collaboration, coordination, and communication skills to support cross-functional interactions and prioritization of activities outside of TM such as assay development, outsourcing, vendor management, biospecimen, data management, biostatistics, and operations teams to align with ICN and strategic stakeholder priorities
• Establish, manage, and maintain cross-functional relationships in coordination with BMS biomarker leads, supporting teams, and relevant stakeholders/technical experts. This includes conducting meetings, organizing agendas, preparing meeting minutes, and following up on action items.
• Proactively manage project risks with a robust understanding of scientific and operational challenges, developing and implementing effective mitigation strategies.
• Escalate significant issues to the Translational Medicine Lead and senior management, as needed
• Establish and maintain a book of work for relevant assets, creating visibility and maintaining transparency into translational activities to key stakeholders that contribute to the overall translational plan for a defined portfolio of assets using effective visualization tools (e.g., Smartsheet, PowerPoint, Office Timeline)
• Oversee the end-to-end ICN budgeted contracts, ensuring alignment with scientific and operational goals. Coordinate with vendor management, alliance management, finance, and global procurement to streamline contract execution and delivery, global procurement and outsourcing management as appropriate to drive from initial draft contract through issuing of purchase orders
• Support the preparation of biomarker study reports and related documentation. Coordinate reviews with biomarker leads and appropriate stakeholders of documents which may support the final clinical study report in relevant SharePoint sites and/or repositories (Verity)
• Coordinate review with biomarker lead and appropriate stakeholders of documents from vendors (e.g., contracts, contract amendments, reports, data transfer agreements) and storage of appropriate final documents in relevant SharePoint sites and/or repositories
• Facilitate publication planning and ensure data delivery for internal/external presentations, publications and conferences, ensuring alignment with strategic timelines
• Support transition of programs internally from early-stage translational team, as needed per program
• Support continuous evolution and measurement of processes and tools to drive efficiency and enhance business value across Translational Development.
• Proactively seek opportunities to leverage and streamline processes and tools to drive improved engagement and program management support.
• Develop and implement agile, creative solutions to solve business challenges within the line organization, across the company, and in partnership with external collaborators.

Associate Director, Translational Program Manager – Immunology, Cardiovascular, Neuroscience

• Uses an understanding of disease biology, the drug development process (particularly cross-functional connectivity), and relevant late-stage challenges (e.g., trends in disease area therapeutic advances, and evolving regulatory, patient advocacy and market access environments) to create a vision for each asset, then design and execute effective development programs in support of the overall R&D portfolio goals.
• Effectively engages cross company expertise and utilizes advisory groups and governance bodies to define, revise and champion asset development strategies and implementation plans.
• Continually analyzes progress, engages in critical thinking, and asserts strong problem-solving toward delivering key data and interpretation essential for robust debate and rapid, data-driven decision making on assigned projects.
• Delivers high quality assets to commercial which have the potential for a competitive profile to address the unmet medical needs of patients and to provide favorable shareholder return.
• Ensures the process and output of the team meets established program standards (per PD&C Process expectations, within budget, on schedule, compliant, etc.), while also looking for opportunities to streamline development and enable continuous improvements without compromising quality.
• Engages senior leaders and functional area stakeholders to ensure alignment of program strategy and operational plans with functional area capabilities, and clearly communicates program risks, implications of changes in the competitive landscape and progress toward key milestones.
• Actively provides input to and drives portfolio level strategy for both internal and external opportunities.
• Participates in regulatory filings (NDA, BLA filings) as well as develops strategy for orphan drug designation.
• Engages with Health Authorities and/or Advisory Committees in the design of clinical trials and endpoints.
• Leads team to develop program strategy and clinical program, commercialization strategy plans, business case development, and understands how access, pricing and reimbursement needs for supporting value proposition will inform trial design.
• Builds and maintains collaborative relationships with external stakeholders (Opinion Leaders, Strategic Alliance Partners, Patient Advocacy Leaders, Health Authorities) and appropriately incorporates insights and advice to maximize program impact.
• Understands clinical trial operational complexities from study start up through enrollment, quality assurance, and study readout.
• Has an active role in analysis and/or interpretation of clinical data and translation into scientific communication strategy, including publications, and commercial strategy.
• Understands and reflects the impact of VAP inputs (Early Access Review and DEX recommendations, commercial opportunity assessment, TOP / TPP requirements, and value drivers as inputs in clinical trial design.
• Actively supports Investor Relations and Public Affairs in managing external BMS communications.
• Integrates commercialization inputs and deliverables to design the late program strategy that enables approval of a meaningfully differentiated asset with potential to maximize asset value.
• Understands necessary commercial inputs needed to inform the end-to-end development process leading to regulatory approval and successful commercialization.
• Integrates market inputs (e.g., TPP, DEX/VAP, CI insights) into the integrated development plan, including clinical plans and labeling strategy; Appreciates translation of clinical data into claims and considerations for label development.
• Understands and contributes to development of forecasts and investment scenarios, how to assess risk and conduct valuations, and implications for decision-making.
• Contributes to the development of brand hallmarks and brand strategy (generic name, brand name, logo, brand colors, positioning, messaging, campaign, segmentation, promotional strategy) understanding the relationship to clinical trial design.
• In partnership with Medical Affairs, supports development of KOL plans and engagements, and leverages KOL input in context of development programs and communicating evidence.
• Supports commercial needs and recommendations to guide CMC and GPS on trade packaging and commercial product.
• Inclusively Collaborates Across the BMS Matrix with an Enterprise Mindset: Effectively collaborates with matrix functions by building trust and driving toward the collective success of the program.
• Demonstrates Enterprise Mindset Problem-Solving and Decision Making: Gathers diverse perspectives assess alternate resolutions and makes thoughtful, informed Enterprise decisions.
• Develops and Leads a High Performing Matrix Team: Builds, leads and inspires high performing cross functional matrix team through a unified program strategy on behalf of our patients.
• Holds Oneself and Others Accountable: Takes initiative to address challenges, removes barriers, holds others accountable for the collective success of the program outcomes and team collaboration.
• Demonstrates Character: Leads with integrity & the values of self-awareness & humility and seeks feedback.

Executive Director, Global Program Lead, Oncology

Vice President

• In support of the Chief Quality Officer, define and shape the Quality strategy for the Global Business Unit (GBU) Manufacturing Quality Network which includes the biologics & pharma operating units, internally and externally, to ensure a high level of cGMP compliance and the safety, efficacy, and quality of all bio and pharma manufactured commercial products.
• Responsible for direction of the quality operations teams supporting manufacturing, laboratory operations, and releasing or certifying of all BMS’ products produced, including internal and external manufacturing.
• This role will ensure consistency and alignment in the overall GBU Network Strategy and operational performance.
• The role will be part of the Global Quality Leadership Team (GQLT), the GBU Leadership Team, and will manage a team of managers, including the Site Quality Heads of internal manufacturing sites, and other Quality Leaders responsible for enabling quality activities critical to compliance and network related projects.
• This role will require strong collaboration with the Global Manufacturing and Supply Chain functions.
• Drive significant impact of current and future business performance and network strategies, through building a functionally excellent infrastructure (knowledge, processes, and systems) to handle moderate to high complexity quality and compliance responsibilities to ensure quality.