Bristol Myers Squibb

Full-stack Engineer

• Design, develop and support a variety of internally developed applications, tools and platforms focused on research data management.
• Contribute to ongoing data management processes with automations fueled by AI/ML, utilizing GenAI, Agentic AI and emerging LLM models.
• Develop and support data pipelines, implement necessary integration work, and manage electronic data collection and access in accordance with BMS policies and project expectations.
• Development and testing of data pipelines, metadata management, lifecycle management, data quality assurance, data management (parsing, transformations, extraction), data enrichment through scripting, and contributing to solution design.
• Develop documentation, APIs, data models, transformation rules to facilitate knowledge of scientific data repositories.
• Collaborate with cross-functional teams to design, develop, and maintain software solutions.
• Explore and integrate AI and LLM technologies for productivity benefits.
• Develop frameworks and automations for managing complex data pipelines, monitor data quality issues and manage data access.
• Provide technical expertise in the capture and transformation of complex scientific data.
• Understand the needs of the business and commit to delivering the best user experience and adoption practices.

Software Engineer II

Manager

Provides comprehensive programming leadership and support to clinical project teams and vendors, including deployment of programming strategies, standards, specifications and programmed analysis to comply with regulatory requirements, SOPs and work practices• Independently develops, validates, troubleshoots, and maintains complex programs and utilities in accordance with predefined specifications and standards• Leads / Supports the electronic submission preparation and review• Develops unambiguous and robust programming specifications (e.g. ADaM specifications)• Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to align with project objectives and ensures clarity and completeness of programming assumptions and requirements; Assesses document robustness and impact on programming activities• Communicates proactively and effectively around issues and risks and contributes to its remediation• Identifies, leads, and supports opportunities to enhance processes and technology• Effectively recruits, manages, develops, evaluates, rewards, motivates, and retains up to 5 direct reports, resulting in an increasing level of capabilities within GBDS• Conducts objective setting, performance check-ins, and year-end discussions in compliance with BMS policies; aligns objectives, feedback and performance evaluation with manager• Meets regularly with direct reports, focusing on project updates, development needs, issue resolution, and provides real-time coaching and feedback; holds staff accountable for quality and timeliness of programming activities; ensures staff is compliant with training requirements• Communicates with manager regarding promotions, performance concerns, and retention risks• Builds and maintains a network with stakeholders and peers to ensure cross-functional strategies and objectives intertwine and build upon each other to achieve results

Senior Manager, Statistical Programming

Therapist

This position combines responsibilities of PROA and Health Outcomes Research Scientist roles. You will define and oversee the execution of clinical outcomes assessment (COA) strategies and implementations for the rigorous development and implementation of patient/clinician reported measures across Cell Therapy portfolio. Support the Executive Director in developing and executing health economic & outcomes research strategy across Cell Therapy assets
PROA: Responsible for implementation of optimal COA strategy including managing research to support the selection, development and validation of COA measures across Cell Therapy portfolio in hematology, immunology and neuroscience therapeutic areas. Support eCOA design and implementation such as providing input to eCOA supplier contracting, kick-off and design meetings, and input in the development of company eCOA standards. Coordinate with functional counterparts in the development and review of eCOA documentation, including data model specifications, project plans, user acceptance testing scripts, device screenshots, site user guides and training slides, and data migration plans. Be an ambassador for PROA and promote the importance of PROA’s role to quantitative and qualitative COA across senior BMS leadership Prepare relevant sections of documents and communications for regulatory agency meetings, support and/or participate in said meetings at regulatory agencies, and provide robust evidence in support of submission activities. Support dissemination of COA results from clinical trials as well as COA development and validation studies that are aligned with publication strategy Participate in creating and delivering education on COA measures for internal business partners
Health Economics and Outcomes Research: Support the development and execution of health economic & outcomes research strategies for CAR T assets throughout early development to post-launch lifecycle Assist in the implementation of HEOR studies and data dissemination activities, such as conducting systematic literature reviews, burden of illness analyses, real-world studies, economic modeling, patient-reported outcomes, and comparative effectiveness studies, as directed Collaborate closely with the Core Value Team to help advance Market Access & Pricing strategy and maintain alignment within the evidence generation plan for Market Access objectives Work as part of cross-functional teams—including clinical development, medical affairs, regulatory, and biostatistics—to ensure HEOR contributions are integrated into overall evidence generation plans Provide input to the management of the CAR T HEOR budgetary plan, helping to optimize the allocation and prioritization of HEOR resources in support of business objectives.

Associate Director, GHEOR Patient-Reported Outcomes Assessment, Cell Therapy

Director

• Lead strategic sponsorship planning and tactical execution by aligning internal teams and building strong relationships with external congress societies to ensure effective execution and results.
• Provide input and maintain accountability for BMS congress standards to ensure consistent, high-quality, and efficient execution across all congress-related activities.
• Support the Congress Excellence Director with the content development of Functional Planning, Annual Congress Strategy Set-Up, and the development of specific strategy objectives as needed.
• Execute the congress pre-planning operations roadmap and assist Senior Managers, Congress Operations and Planning as needed.
• Lead congress planning as an Engagement Lead or Tactical Lead, as defined by the Director, while concurrently coordinating multiple Tier 1 and Tier 2 congresses, demonstrating exceptional multitasking and strategic oversight.
• Lead governance processes in partnership with the CE Director and ensure full compliance with global and local regulations by partnering closely with legal and compliance teams.
• Leads and delivers congress communications and briefings.
• Engage proactively with cross functional colleagues to enhance planning and execution in all phases of the congress to drive continuous process improvement.
• Design and implement innovative approaches to enhance customer experience at congresses.
• Develop and implement Thought Leader Encounter strategies in collaboration with cross-functional teams, while leading the planning, coordination, and budget management for their execution at congresses.
• Lead overall booth exhibition, including booth planning, development of materials, booth staffing and budget management.
• Travel as needed to ensure successful execution and implementation of congresses.
• Model BMS behaviors and company values at all organizational levels, serving as a role model and advocate.

Associate Director, Congress Engagement

Managers of Statistical programming provide comprehensive programming expertise to clinical project teams to support the development, regulatory approval and market acceptance of Bristol Myers Squibb (BMS) products.
This position is primarily responsible for the design, development and implementation of technical solutions for integrating, analyzing and reporting clinical data.
Managers of Statistical Programming develop collaborative relationships and work effectively within Global Biometrics & Data Sciences (GBDS), with external vendors and members of cross-functional development teams.
Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures; Perform programming validation to ensure quality of analysis datasets and programming outputs
Provides comprehensive programming support for project teams, including development of programming strategies, standards, specifications and programmed analysis
Support the electronic submission preparation and review
Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements; Assesses impact on programming activities
Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers
Provides leadership for ensuring quality of Global Biometric and Data Sciences (GBDS) deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices
Identifies opportunities for increased efficiency and consistency within GBDS and our interactions with strategic vendors
Independently leads and / or performs programming assignments across multiple projects with minimal supervision

Manager, Statistical Programming

• Oversees global policy adherence, uses performance analytics, manages risks, and enhances customer experiences while handling high volumes of global transactions.
• Leading a cross-functional team, maintaining effective global controls, ensures regulatory compliance, and drives process improvements.
• Utilizing advanced technologies, aiming for cost efficiency and value creation while engaging with internal and external stakeholders to strengthen leadership in process management and supplier engagement.
• By offering strategic direction and promoting operational excellence, advancing the company's global financial operations and ensures sustainable success.
• Strategic Ownership & Governance: Develop and execute the global R2R strategy to align with organizational goals and priorities.
• Define and enforce global R2R policies, procedures, and standards while ensuring adherence to local regulations and requirements.
• Act as the global escalation point for R2R-related issues, ensuring timely resolution and stakeholder satisfactions.
• Process Optimization & Continuous Improvement Drive process standardization and harmonization across regions, leveraging technology and best practices.
• Identify opportunities to eliminate inefficiencies, reduce costs, and improve cycle times within R2R processes.
• Lead digital transformation initiatives, such as automation, AI, and analytics tools, to enhance process capabilities.
• Performance Management Conduct regular reviews of process performance with Stakeholders, identifying and addressing gaps or opportunities for improvement.
• Collaboration & Stakeholder Management Partner with Finance, IT, and other key stakeholders to ensure seamless integration of R2R process into end–to– end operations.
• Build strong relationships with external service providers.
• Risk Management & Compliance Ensure compliance with all internal policies, external regulations, and audit requirements related to R2R processes.
• Develop and maintain a strong internal control framework to mitigate risks within the R2R function.
• Leadership & Team Development Mentor and guide regional R2R leads and teams. Fostering a culture of accountability. Collaboration, and continuous learning.
• Manage up to ten (10) direct reports up to Associate Director level.
• Lead change management initiatives to drive adoption of process changes across the organization.

Director, Record to Report Global Process Owner

Auditor

• Senior Auditor in GIA will work in a team environment to plan and execute dynamic risk-based audits and identify value-added recommendations to strengthen Company processes and controls.\n• Audits will include U.S.-based operations, international Company subsidiaries, strategic initiatives, critical business processes, and key third-party outsourcing arrangements.\n• Throughout the audits, the Senior Auditor will have the opportunity to interact with senior management and enhance oral and written communication skills.\n• Lead meetings involving various levels of management to effectively communicate audit status, align on significant audit issues and recommended corrective actions.\n• Prepare clear, detailed audit documentation evidencing the results of actual testing procedures in accordance with BMS and the Institute of Internal Auditors (IIA) standards.\n• Prepare audit reports, including clearly written, concise audit observations that effectively communicate identified issues and their related corrective actions to key stakeholders.\n• Participate with the team in trainings and regular departmental meetings that include sharing best practices.\n• Participate in departmental projects as assigned (e.g., audit lessons learned, training, continuous improvement, etc.).

Senior Auditor, Global Internal Audit & Assurance

Consultant

• As part of the commercial organization, the Clinical Nurse Consultant (CNC) is a trusted clinical expert responsible for developing professional relationships and educating key Health Care Professionals (HCP) involved in the care of patients receiving BMS hematology products in a defined geography.\n• The primary role of the CNC is to drive peer to peer interactions with customers that optimize patient outcomes by delivering end-to-end clinical exchanges that clarify the complexities of patient identification and management.\n• The purpose of these interactions is to deliver a continuum of clinical education and support that address the needs of HCPs starting or continuing patients on BMS hematology and oncology medicines, optimizing patient management and duration of treatment.\n• CNCs also educate on unmet disease needs and discuss the current treatment landscape for these patient populations.\n• CNC interactions are aligned with on-label commercial strategies and the needs expressed by customers.\n• CNCs may develop relationships with oncology focused Patient Support Groups for the purpose of presenting approved presentations that address specific patient education needs identified by the group leader.\n• CNCs are viewed as clinical experts by their customers for the BMS hematology and oncology portfolio.\n• Product responsibilities may change based on franchise and business needs.\n• Customer Focus: Develop and maintain relationships with academic and community HCPs within assigned geography to provide on-label clinical and product education for BMS hematology and oncology products.\n• The CNC will use various channels for interactions (1:1, group presentations, remote, etc.) while utilizing on-label approved marketing materials.\n• Actively assess the treatment and patient management landscape by meeting with HCPs to understand their needs and current patient management processes/protocols.\n• Demonstrate proficiency in using available on-label CNC resources and presentations.\n• Effectively utilize platform skills for presenting information to HCPs and be able to respond to questions, ensuring accuracy and compliance with local procedures, ethical and legal-guidelines and directives.\n• Consistently evaluate the impact of CNC activities in an account and plan for follow-up or next steps.\n• Respond and adapt quickly to support new and ongoing educational gaps or other customer needs.\n• Actively monitor CNC dashboard & account data, adjusting activities and business plans to meet goals and objectives.\n• Continuously seek to increase knowledge of treatment landscape, product attributes and disease states.\n• Actively prepare to address the educational needs of customers.\n• Provide Clinical Expertise: In collaboration with commercial partners, deliver on-label educational speaker programs to HCP customers in approved out of office settings.\n• In collaboration with commercial, deliver on-label educational in-services for HCP customers.\n• Provide product demonstrations and infusion support for CAR T sites starting new patients.\n• Support initial and ongoing clinical/disease area and product specific training to internal stakeholders (e.g. Commercial, Value Access & Payment).\n• Participate in assigned Medical Congress activities.\n• Share clinical insights and patient management experiences internally to support franchise strategy.\n• Commercial Planning and Execution: Adopt account business planning approach and contribute to cross-functional business plans.\n• Assist with the development of clinically meaningful CNC programs/projects in line with commercial strategies and plans.

Clinical Nurse Consultant

• Leads all elements of internal Competitive Intelligence (CI) model for BMS’ Cell Therapy (CT) franchise based on consultative engagement with key stakeholders, leading internal intelligence networks, coordinating the communication of intelligence, leading external CI vendors/partners, and leveraging relevant internal tools and platforms.
• Conducts analysis and research based on stakeholder-driven key intelligence questions while adhering to consistency and set standards across BMS.
• Builds relationships and effectively influences all senior management stakeholders to advance the culture of insight-enabled decision making.
• Identifies, gathers, synthesizes, and distills information/intelligence into key insights across the cell therapy portfolio and in partnership with cross matrix business partners.
• Advances initiatives, applies successful pilots across Cell Therapy and ensures consistency amongst strategic CI capabilities (e.g., field intelligence synthesis, congress coverage, competitive simulation workshops).
• Translates insights into actionable recommendations for US and WW Commercial, Strategy, Medical, and in support of EA and BP initiatives.
• Maintains forensics capability (asymmetric intelligence) via extrapolation, triangulation and internal expert validation.
• Executes all projects within budget assigned, in a timely fashion, making tradeoffs as necessary.
• Ensures appropriate dissemination of, and access to, competitive intelligence so it may be fully leveraged to answer strategic questions.
• Demonstrates, and holds others accountable to high standards of business integrity.
• Responds to senior-level ad-hoc business questions with expert analysis and timely delivery.
• Assesses vendor capabilities by research type and strives to define most effective CI model to drive efficiencies, prioritization, and simplification across the CT commercialization CI team.
• Leads Cell Therapy CI indirect reports, balancing company portfolio prioritization with capacity while keeping individual development goals and skill sets in mind; coaches and mentors indirect reports.

Director, Cell Therapy Competitive Intelligence

• Position Summary: The Associate Director, Oncology & Hematology - will: Support relationships with external thought leaders and, with the input of internal stakeholders, assist with strategies to successfully advance external research that will accelerate the development of BMS’s pipeline.
• Contribute to the engagement with investigators to bring concepts to full proposals and aid in site assessment/recommendation, facilitation of study design, presentation to governance in partnership with disease area leads.
• Be responsible for the overall project leadership throughout the lifecycle of the studies.
• Key Responsibilities: Facilitate collaborative exchange between BMS and thought leaders in community practice and academia, including scientific dialogue and representing BMS as a trusted, inclusive, and innovative industry collaborator and partner of choice.
• Be accountable for delivery of MEG studies from concept ideation to governance approval and throughout the study lifecycle.
• Act as point of contact for MEG studies within Therapeutic and Disease area teams.
• Aid in strategy development to accelerate the development of BMS’s clinical development pipeline leveraging external research platforms, technologies, and insights.
• Align with functional and therapeutic area stakeholders on new external opportunities that will inform strategy and influence decisions in the creation/refinement of integrated evidence generation plans.
• Lead projects leveraging relevant disease subject matter expertise.
• Contribute to the evolution of MEG therapeutic/disease area strategy and value proposition.